← Back to catalogue

Chs

FDA UDI

Class I (US FDA UDI)

by Canadian Hospital Specialties Limited

Identity

Trade Name
CHS FDA UDI
Generic Name
Bedpan FDA UDI
Device Name
6.5OZ SPECIMEN PP WITH PAPER LID FDA UDI
Model / Reference
UC1007PP FDA UDI
Description
6.5OZ SPECIMEN PP WITH PAPER LID FDA UDI

Identifiers

Catalog Number
UC1007PP FDA UDI
Primary DI / UDI-DI
50628725096730 FDA UDI
FDA Product Code
FOB FDA UDI
GMDN Term
Bedpan FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Category: Bedpan

Chs by Canadian Hospital Specialties Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedpan.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0f4aefb8-c5f9-4b32-a13d-3c18aa6c5e80 35 fields · synced May 30, 2026