N/A Kt-A02

by wenzhou dongfang medical instrument co., ltd 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number06970784670048 UDI-DI	Date25 Mar 2022Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Blood pressure cuff, reusable
Model / Reference: KT-A02

Primary DI / UDI-DI: 06970784670048
510(k) Number: K081951
FDA Product Code: DXQ
GMDN Term: Blood pressure cuff, reusable

Device Class: Class II
Regulation Number: 870.1120
GUDID distribution status: In Commercial Distribution

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Properties

Lot / Batch Number
Expiration Date

Other properties (12)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Manufacturing Date: No