← Back to catalogue

Welch Allyn, Inc.

FDA UDI

Class II (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Transportable medical equipment stand, non-powered FDA UDI
Device Name
Quick Disconnect, plastic socket for S12/S19 FDA UDI
Model / Reference
901189 FDA UDI
Description
Quick Disconnect, plastic socket for S12/S19 FDA UDI

Identifiers

Catalog Number
8363-021-50 FDA UDI
Primary DI / UDI-DI
00732094277036 FDA UDI
510(k) Number
K173765 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
Transportable medical equipment stand, non-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Transportable medical equipment stand, non-powered

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

Similar devices

Also classified as Transportable medical equipment stand, non-powered.

Cleared under the same submission

K173765 also covers:

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

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI 3c36d63e-f11f-49fe-8608-a8f279b10018 36 fields · synced May 31, 2026