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Direct Supply

FDA UDI

Class II (US FDA UDI)

by Hoffmann NOA Medical Industries, LLC

Identity

Trade Name
Direct Supply FDA UDI
Generic Name
Bed mattress support platform, electric FDA UDI
Device Name
ASSIST DEVICE - ZOA - Pivoting (Beige) FDA UDI
Model / Reference
7520018BEI FDA UDI
Description
ASSIST DEVICE - ZOA - Pivoting (Beige) FDA UDI

Identifiers

Primary DI / UDI-DI
00817492013179 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Bed mattress support platform, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bed mattress support platform, electric

Direct Supply by Hoffmann NOA Medical Industries, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed mattress support platform, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b76f75c4-367f-454e-8fc2-438581af13b4 33 fields · synced Jun 6, 2026