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Flents Protechs

FDA UDI

Class U (US FDA UDI)

by Apothecary Products, Inc.

Identity

Trade Name
FLENTS PROTECHS FDA UDI
Generic Name
Earplugs, single-use FDA UDI
Device Name
PROTECHS SLEEP EAR PLUGS 10 PR 6/72 FDA UDI
Model / Reference
68050 FDA UDI
Description
PROTECHS SLEEP EAR PLUGS 10 PR 6/72 FDA UDI

Identifiers

Primary DI / UDI-DI
00025715680507 FDA UDI
FDA Product Code
EWD FDA UDI
GMDN Term
Earplugs, single-use FDA UDI

Classification

Device Class
U 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

Yes

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: Earplugs, single-use

Flents Protechs by Apothecary Products, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Earplugs, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4fe90641-806b-4320-8dff-a57e8d6b295d 34 fields · synced May 30, 2026