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Medline PAD9160

by Medline Industries, Inc.

Medline PAD9160 is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 6 May 2022 (UDI-DI 10193489082517), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10193489082517 UDI-DI Date6 May 2022ListedStatusListed 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  • Withdrawn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
Medline
Generic name
Electrosurgical return electrode, single-use
Model / Ref / Catalog
PAD9160
Primary DI / UDI-DI
10193489082517
FDA product code
GEI
GMDN term
Electrosurgical return electrode, single-use
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrosurgical return electrode, single-use

Similar devices in this category

Other devices filed under Electrosurgical return electrode, single-use.

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)