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oneNEST M

FDA UDI

Class II (US FDA UDI)

by Umano Medical Inc

Identity

Trade Name
oneNEST M FDA UDI
Generic Name
Alternating-pressure bed mattress FDA UDI
Device Name
303-M803508HS2FB-BIL oneNEST M is a powered mattress 80'' x 35'' 2 ways. It can be used with or without control unit. FDA UDI
Model / Reference
303-M803508HS2FB-BIL FDA UDI
Description
303-M803508HS2FB-BIL oneNEST M is a powered mattress 80'' x 35'' 2 ways. It can be used with or without control unit. FDA UDI

Identifiers

Catalog Number
303-M803508HS2FB-BIL FDA UDI
Primary DI / UDI-DI
00670482000777 FDA UDI
FDA Product Code
IOQ FDA UDI
GMDN Term
Alternating-pressure bed mattress FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5170 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Alternating-pressure bed mattress

oneNEST M by Umano Medical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure bed mattress.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Umano Medical Inc

Sources (1)

  • FDA UDI be8b3c86-1921-4024-8013-b0276a32a004 34 fields · synced Jun 1, 2026