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Pmi P0113M

by Progressive Medical, Inc.

Pmi P0113M is a Class II device made by Progressive Medical, Inc., listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00812608020812), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00812608020812 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pmi
Generic name
Endoscopic electrosurgical electrode, bipolar, single-use
Model / Ref / Catalog
P0113M
Primary DI / UDI-DI
00812608020812
FDA product code
GEI
GMDN term
Endoscopic electrosurgical electrode, bipolar, single-use
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic electrosurgical electrode, bipolar, single-use

Similar devices in this category

Other devices filed under Endoscopic electrosurgical electrode, bipolar, single-use.

Other devices from Progressive Medical, Inc.

See all devices from Progressive Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)