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S/S Tubular frame maternity bassinet

FDA UDI

Class II (US FDA UDI)

by Imperial Surgical Ltd

Identity

Trade Name
S/S Tubular frame maternity bassinet FDA UDI
Generic Name
Neonatal bed FDA UDI
Device Name
A stainless steel tubular frame bassinet for use in the operating room and/or maternity suite. FDA UDI
Model / Reference
PH-2655 FDA UDI
Description
A stainless steel tubular frame bassinet for use in the operating room and/or maternity suite. FDA UDI

Identifiers

Catalog Number
ph-2655 FDA UDI
Primary DI / UDI-DI
07540162040054 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
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

Yes

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

No

FDA UDI

Category: Neonatal bed

S/S Tubular frame maternity bassinet by Imperial Surgical Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neonatal bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 36eabad3-a326-4436-bf7a-e0dd1ac2111f 34 fields · synced May 30, 2026