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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Breathing mouthpiece, single-use FDA UDI
Device Name
MOUTHPIECE,WHITE,FITS 28-32MM FDA UDI
Model / Reference
DYNJ754 FDA UDI
Description
MOUTHPIECE,WHITE,FITS 28-32MM FDA UDI

Identifiers

Catalog Number
DYNJ754 FDA UDI
Primary DI / UDI-DI
20888277716718 FDA UDI
FDA Product Code
BYP FDA UDI
GMDN Term
Breathing mouthpiece, single-use 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

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

No

FDA UDI

Category: Breathing mouthpiece, single-use

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing mouthpiece, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b1b1aebd-42af-4a0a-b690-a89406d21300 35 fields · synced May 30, 2026