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Pro Advantage

FDA UDI

Class II (US FDA UDI)

by National Distribution & Contracting, Inc.

Identity

Trade Name
Pro Advantage FDA UDI
Generic Name
Aneroid manual sphygmomanometer FDA UDI
Device Name
Pro Advantage Aneroid Sphyg Pocket Adult Black Latex Free Premium each FDA UDI
Model / Reference
P548340 FDA UDI
Description
Pro Advantage Aneroid Sphyg Pocket Adult Black Latex Free Premium each FDA UDI

Identifiers

Catalog Number
P548340 FDA UDI
Primary DI / UDI-DI
M220P5483403 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

No

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

No

FDA UDI

Category: Aneroid manual sphygmomanometer

Pro Advantage by National Distribution & Contracting, 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

Sources (1)

  • FDA UDI 79cb607a-161b-4949-a3ad-486fe144b0db 35 fields · synced Jun 6, 2026