The neoBLUE cozysystem is positioned underneath the baby to deliver phototherapy via a blue LED light source. NeoBLUE blanket available with optional hardware for pole-mounting applications Most effective degradation of bilirubin1 The neoBLUE cozy system meets AAP Guidelines for intensive phototherapy2. Library Alpine Biomed Natus LED Phototherapy manuals, recalls & alerts incl neoBLUE Radiometer User Manual Rev C, neoBLUE LED Phototherapy Systems Manual Addendum March 2018, neoBLUE Radiometer User Manual Rev D, neoBLUE LED Phototherapy Technical Bulletin Sept 2016 - System Performance Update, neoBLUE LED Phototherapy System Quick Guide April 2016, neoBLUEcozy Service Manual Rev A.
- Neoblue Led Phototherapy Manual
- Neoblue Led Phototherapy Radiometer Manual
- Natus Neoblue Led Phototherapy Manual
- Neoblue Led Phototherapy System User Manual Template
- If necessary, use the adjustment tool to adjust potentiometer B for a light intensity of 15 ± 2 µW/cm /nm. If the tolerances in steps 4 and 5 in Section 2.3.2 are met, the UUT can be returned to the user. ® neoBLUE LED Phototherapy System Service Manual PN 001320 Rev K.
- The neoBLUE blanket system is positioned underneath the baby to deliver phototherapy via a blue LED light source and fiberoptic blanket. NeoBLUE® radiometer The neoBLUE radiometer accurately measures the intensity of neoBLUE® LED Phototherapy Systems providing precise measurement of light in the blue spectrum to ensure optimal phototherapy.
- The advanced LED phototherapy system from Delta Medical International offers unbeatable performance for bilirubin therapy. The product has high light output, large area of illumination and a combination of numerous other unique features to provide most effective treatment.
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DESCRIPTION
The neoBLUE LED Phototherapy System consists of two products – the neoBLUE Phototherapy light source and the neoBLUE Phototherapy Roll Stand![Led Led](https://images.dotmed.com/images/listingpics/2172490_3.jpg)
The neoBLUE blanket system is positioned underneath the baby to deliver phototherapy via a blue LED light source & fiberoptic blanket. The neoBLUE blanket system meets AAP Guidelines for intensive, efficacious phototherapy. Delivers phototherapy over a larger effective treatment area than other fiberoptic devices.
FORUMSView All (8)
Ask a New Question0Replies6 months ago | 6 months agoquestion We have the neoblue blanket. The mattress was taken off the unit before educating staff on use. Which side does the air bubble mattress go onto?Reply |
-ALBMET 2 years ago | 2 years agoQuestion regarding Power Connector on unit Greetings all, hope I can get a quick correct answer. the power connector on the NeoCozy Blue is loose. Is there or does anyone know what type of glue this would be ? It looks like regular epoxy but I would hate to guess wrong. Concern is over patient safety, Natus says they can repair but the cost seems a bit much. let me know, Thanks!Please see link for reference!http://www.natus.com/index.cfm?page=products_1&crid=769Reply |
2Replies2 years ago | 2 years agoNatus - neoBLUE cozy service manual Can anybody help me with service manual on Natus - neoBLUE cozy?Reply |
Neoblue Led Phototherapy Manual
DOCUMENTS / MANUALSView All
Neoblue Led Phototherapy Radiometer Manual
FEATURES
- The neoBLUE LED does not emit light in the ultraviolet (UV) range — reducing the potential risk of skin damage
- The neoBLUE LED does not emit light in the infrared radiation (IR) range — reducing the potential risk of fluid loss
- Device automatically shuts off in the event of light box overheating
- Flashing indicator light alerts user to check for blocked air vents
- Streamlined, oval design conforms to the shape of the baby
- Large and small blanket sizes available
- Mattress provides comfortable cushioning underneath the infant
- Disposable mattress covers ensure clean, soft surface for baby
- Blanket rolls or bumpers can be used as desired for added positioning & cushioning around the baby
- A blanket can be used in conjunction with the neoBLUE blanket for added warmth & comfort
- Baby can be held or nursed without interrupting phototherapy, encouraging infant-parent bonding
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Natus Neoblue Led Phototherapy Manual
Neoblue Led Phototherapy System User Manual Template
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Device Design | |||||||||||||||||||||||||
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Natus began sending the URGENT RECALL NOTIFICATION / FIELD SAFETY NOTICE neoBLUE blanket system performance letter dated October 27, 2016 and the Technical Bulletin to US customers on October 28, 2016. Natus plans to notify their international customers on December 2, 2016. Customers were informed in March 2015 of a potential issue of discoloration/degradation/melting of the fiber optic bundle at the pad connector which is inserted in the neoBLUE blanket light box. Included with that letter was a Technical Bulletin which described the issue and addressed many of your potential questions. The purpose of this current letter (dated October 27, 2016) is to communicate Natus' plan for a follow-on field correction for neoBLUE blanket systems shipped between 2011 through March 21, 2016 (Serial Numbers up to and including xxxx004282), and to remind customers of the instructions contained in the neoBLUE blanket Technical Bulletin. Natus is in the process of confirming an updated neoBLUE blanket configuration which will not be susceptible to the degradation described above. However, the date of project completion is uncertain at this time. Natus will contact customers when the new configuration is available, at which time Natus intend to initiate a field corrective action to replace or upgrade your device(s). Please contact Natus [email protected] if you have any further questions. Please call (800) 426-0353. | |||||||||||||||||||||||||
2619 units (1925 units in the US and 694 units OUTSIDE the US) | |||||||||||||||||||||||||
Worldwide Distribution - USA (nationwide) Distribution and to the countries of : including American Samoa and Guam, and in the following countries: Albania, Argentina, Australia, Austria, Bangladesh, Canada, Chile, Costa Rica, Croatia, Czech Republic, Denmark, Ecuador, Finland, France, Germany, Hong Kong, Indonesia, Iraq, Israel, Italy, Korea, Kuwait, Latvia, Malaysia, Mongolia, Namibia, Netherlands, Nigeria, Norway, Panama, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Singapore, Slovakia (Slovak Republic), Slovenia, South Africa, Spain, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Uruguay, Viet Nam, and Virgin Islands (British). | |||||||||||||||||||||||||
TPLC Device Report | |||||||||||||||||||||||||
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes. | |||||||||||||||||||||||||
510(K) Database | 510(K)s with Product Code = LBI and Original Applicant = NATUS MEDICAL INCORPORATED |