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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
Patient monitoring system module, blood pressure, invasive FDA UDI
Device Name
ProBP 2000 Digital BP Device, PLUS, NA FDA UDI
Model / Reference
901123 FDA UDI
Description
ProBP 2000 Digital BP Device, PLUS, NA FDA UDI

Identifiers

Catalog Number
2000 PLUS-A FDA UDI
Primary DI / UDI-DI
06932825304237 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Patient monitoring system module, blood pressure, invasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 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

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: Patient monitoring system module, blood pressure, invasive

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

Similar devices

Also classified as Patient monitoring system module, blood pressure, invasive.

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 91c4d9bc-d7f5-4d7f-9112-fb96c25874a2 35 fields · synced May 30, 2026