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Welch Allyn, Inc.

FDA UDI

Class II (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Earphone cushion FDA UDI
Device Name
MICROTYMP 3 TIPS - 4 MEDIUM BLUE FDA UDI
Model / Reference
901001 FDA UDI
Description
MICROTYMP 3 TIPS - 4 MEDIUM BLUE FDA UDI

Identifiers

Catalog Number
406512 FDA UDI
Primary DI / UDI-DI
00732094048414 FDA UDI
FDA Product Code
ETY FDA UDI
GMDN Term
Earphone cushion FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1090 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Earphone cushion

Welch Allyn, Inc. by Welch Allyn, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Earphone cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI 0150005c-886c-4805-aa10-b5feccf238f2 35 fields · synced May 30, 2026