← Back to catalogue

Adcuff™

FDA UDI

Class II (US FDA UDI)

by American Diagnostic Corporation

Identity

Trade Name
Adcuff™ FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
D-Bar Cuff & Bladder, 2 Tube,,Lrg Adult, Navy, LF FDA UDI
Model / Reference
845-790-12XN-2 FDA UDI
Description
D-Bar Cuff & Bladder, 2 Tube,,Lrg Adult, Navy, LF FDA UDI

Identifiers

Catalog Number
845-790-12XN-2 FDA UDI
Primary DI / UDI-DI
00634782070878 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
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

No

FDA UDI

Category: Blood pressure cuff, reusable

Adcuff™ by American Diagnostic Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, reusable.

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

Sources (1)

  • FDA UDI 6d6a34a8-d2b6-47a7-a541-a29ab0c9dbd3 37 fields · synced May 30, 2026