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Clement Clarke International

FDA UDI

Class I (US FDA UDI)

by Clement Clarke International Limited

Identity

Trade Name
Clement Clarke International FDA UDI
Generic Name
Breathing mouthpiece, reusable FDA UDI
Device Name
UNIVERSAL M/PIECES IN BAG X15 FDA UDI
Model / Reference
3103095 FDA UDI
Description
UNIVERSAL M/PIECES IN BAG X15 FDA UDI

Identifiers

Primary DI / UDI-DI
05023323029522 FDA UDI
FDA Product Code
BYP FDA UDI
GMDN Term
Breathing mouthpiece, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5620 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

Yes

FDA UDI

Category: Breathing mouthpiece, reusable

Clement Clarke International by Clement Clarke International Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing mouthpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 517d885e-7973-4b00-a70e-961c9cdd87dd 33 fields · synced May 30, 2026