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Erbe 20192-125

by Erbe Elektromedizin GmbH

Erbe 20192-125 is an electrical-only medical device connection cable (FDA Class II; FDA product code GEI, Electrosurgical, Cutting & Coagulation & Accessories) made by Erbe Elektromedizin GmbH, cleared under FDA 510(k) K083452 on 31 Dec 2008 (1 earlier submission) and listed in FDA GUDID since 22 Sep 2016 (UDI-DI 04050147005051), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04050147005051 UDI-DI Date22 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK083452 Date31 Dec 2008DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K083452 decided 31 Dec 2008 Active· +1 more in the status table
  • FDA GUDID UDI-DI 04050147005051 listed 22 Sep 2016 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K023886
  2. Cleared FDA 510(k) K083452
  3. Listed FDA GUDID 04050147005051

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Erbe
Generic name
Electrical-only medical device connection cable, reusable
Model / Ref / Catalog
20192-125
Primary DI / UDI-DI
04050147005051
510(k) Number
FDA product code
GEI
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)