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Blood Pressure Cuff

FDA UDI

Class II (US FDA UDI)

by Avante

Identity

Trade Name
Blood Pressure Cuff FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
ADULT SINGLE LUMEN 27-35CM FDA UDI
Model / Reference
80031ABL FDA UDI
Description
ADULT SINGLE LUMEN 27-35CM FDA UDI

Identifiers

Primary DI / UDI-DI
00815871022460 FDA UDI
510(k) Number
K143728 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

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: Blood pressure cuff, reusable

Blood Pressure Cuff by Avante — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avante

Sources (1)

  • FDA UDI d203ca44-ae70-48cd-9f7a-65dc5a6fd582 35 fields · synced Jun 1, 2026