MytaMed ME3603-00

by Mytamed, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00841019110218 UDI-DI	Date10 Jul 2016Listed	StatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: MytaMed
Generic Name: Open-surgery electrosurgical electrode, monopolar, single-use
Model / Reference: ME3603-00

Primary DI / UDI-DI: 00841019110218
510(k) Number: K100912
FDA Product Code: GXZ
GMDN Term: Open-surgery electrosurgical electrode, monopolar, single-use

Device Class: Class II
Regulation Number: 882.1350
GUDID distribution status: Not in Commercial Distribution

Sterilization Method: Radiation Sterilization

Properties

Sterile
Single Use
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (9)

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