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Well Baby Bassinet

FDA UDI

Class II (US FDA UDI)

by Datex-Ohmeda Inc.

Identity

Trade Name
Well Baby Bassinet FDA UDI
Generic Name
Neonatal bed FDA UDI
Device Name
ASSY-LAU, BASSINET WITH TUB NAT OAK, WITH LABELS MANUFACTURING ASSEMBLY - MAKE FDA UDI
Model / Reference
BN6 FDA UDI
Description
ASSY-LAU, BASSINET WITH TUB NAT OAK, WITH LABELS MANUFACTURING ASSEMBLY - MAKE FDA UDI

Identifiers

Primary DI / UDI-DI
00840682119429 FDA UDI
FDA Product Code
NZG FDA UDI
GMDN Term
Neonatal bed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5145 FDA UDI
Commercial Distribution
Not 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

Yes

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

Well Baby Bassinet by Datex-Ohmeda Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Datex-Ohmeda Inc.

Sources (1)

  • FDA UDI ae98f933-8cd6-4f0c-93d4-634243fbaf21 35 fields · synced May 30, 2026