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Medviron Bassinet

FDA UDI

Class II (US FDA UDI)

by Medviron Llc

Identity

Trade Name
Medviron Bassinet FDA UDI
Generic Name
Infant-hammock bed mattress FDA UDI
Device Name
Michigan Bassinet 2 Drawer FDA UDI
Model / Reference
Michigan Bassinet 2 Drawer FDA UDI
Description
Michigan Bassinet 2 Drawer FDA UDI

Identifiers

Catalog Number
M25-0000-0000 FDA UDI
Primary DI / UDI-DI
10851477007125 FDA UDI
FDA Product Code
NZG FDA UDI
GMDN Term
Infant-hammock bed mattress FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5145 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: Infant-hammock bed mattress

Medviron Bassinet by Medviron Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infant-hammock bed mattress.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medviron Llc

Sources (1)

  • FDA UDI a8724dd4-c593-4e6a-8d76-406d4cccaead 35 fields · synced Jun 8, 2026