← 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
Blood pressure cuff, reusable FDA UDI
Device Name
Welch Allyn Trimline Blood Pressure Cuff; Size-11 Adult, Reusable, 1-Tube (10.0 in/25.4 cm), Female Luer-Slip (#1391) Connector FDA UDI
Model / Reference
901043 FDA UDI
Description
Welch Allyn Trimline Blood Pressure Cuff; Size-11 Adult, Reusable, 1-Tube (10.0 in/25.4 cm), Female Luer-Slip (#1391) Connector FDA UDI

Identifiers

Catalog Number
1953S FDA UDI
Primary DI / UDI-DI
00732094015430 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Blood pressure cuff, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

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 23c1f9a0-dd42-4a0b-b5bd-e0419f9d1297 36 fields · synced May 30, 2026