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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
Aneroid manual sphygmomanometer FDA UDI
Device Name
Welch Allyn Tycos DS44 Pocket Aneroid Sphygmomanometer with DuraShock Gear Free, Shock Resistant Technology; Inmetro Certification, 5-Year Calibration Warranty, Inflation Bulb and Valve; Size-11 Adult, Reusable (Two Piece), 1-Tube Cuff FDA UDI
Model / Reference
901092 FDA UDI
Description
Welch Allyn Tycos DS44 Pocket Aneroid Sphygmomanometer with DuraShock Gear Free, Shock Resistant Technology; Inmetro Certification, 5-Year Calibration Warranty, Inflation Bulb and Valve; Size-11 Adult, Reusable (Two Piece), 1-Tube Cuff FDA UDI

Identifiers

Catalog Number
DS44-11CBT FDA UDI
Primary DI / UDI-DI
00732094085488 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Aneroid manual sphygmomanometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Aneroid manual sphygmomanometer

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

Similar devices

Also classified as Aneroid manual sphygmomanometer.

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 4ecd5351-02f6-4dc9-a548-9f13f8f98e19 35 fields · synced May 30, 2026