Unimed P21079P

by Unimed Medical Supplies, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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	Number06936735464036 UDI-DI	Date17 Aug 2022Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Unimed
Generic name: Electrocardiographic lead set, reusable
Model / reference: P21079P

Primary DI / UDI-DI: 06936735464036
FDA product code: DSA
GMDN term: Electrocardiographic lead set, reusable

Device class: Class II
Regulation number: 870.2900
GUDID distribution status: In Commercial Distribution

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Properties

Lot / batch number
Manufacturing date

Other properties (13)

Supplied sterile: No
Sterilise before use: 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
Expiration date: No