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Valeo Vbr 030.8100

by CTL Medical Corporation

Valeo Vbr 030.8100 is a Class II device made by CTL Medical Corporation, cleared under FDA 510(k) K073505 on 9 Jan 2008 and listed in FDA GUDID since 21 Jun 2024 (UDI-DI 00841732129740), active as of 22 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 22 Oct 2026

Documents

510(k) K073505

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841732129740 UDI-DI Date21 Jun 2024ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK073505 Date9 Jan 2008DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K073505 decided 9 Jan 2008 Active
  • FDA GUDID UDI-DI 00841732129740 listed 21 Jun 2024 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K073505
  2. Listed FDA GUDID 00841732129740

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Valeo Vbr
Generic name
Device sterilization/disinfection container, reusable
Model / reference
030.8100
Primary DI / UDI-DI
00841732129740
510(k) Number
FDA product code
MQP
GMDN term
Device sterilization/disinfection container, reusable
Device class
Class II
Regulation number
888.3060
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

  • Sterilise before use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)