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Erbe 20150-300

by Erbe Elektromedizin GmbH

Erbe 20150-300 is a Class II device made by Erbe Elektromedizin GmbH, cleared under FDA 510(k) K072404 on 31 Oct 2007 and listed in FDA GUDID since 11 Oct 2016 (UDI-DI 04050147001930), 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

510(k) K072404

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04050147001930 UDI-DI Date11 Oct 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Abbreviated NumberK072404 Date31 Oct 2007DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K072404 decided 31 Oct 2007 Active
  • FDA GUDID UDI-DI 04050147001930 listed 11 Oct 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K072404
  2. Listed FDA GUDID 04050147001930

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  • Withdrawn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
Water jet knife system pump-cartridge
Model / Ref / Catalog
20150-300
Primary DI / UDI-DI
04050147001930
510(k) Number
FDA product code
FQH
GMDN term
Water jet knife system pump-cartridge
Device class
Class II
Regulation number
880.5475
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FQH (LAVAGE, JET).

Other devices from Erbe Elektromedizin GmbH

See all devices from Erbe Elektromedizin GmbH →

Properties

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