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Kbmed Cap-TT1275P

by KB Medical (group), Inc.

Kbmed Cap-TT1275P is a Class I device made by KB Medical (group), Inc., listed in FDA GUDID since 22 May 2025 (UDI-DI 00810100050559), 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 Number00810100050559 UDI-DI Date22 May 2025ListedStatusListed 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  • Withdrawn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
Kbmed
Generic name
Test tube/reservoir cap
Model / reference
CAP-TT1275P
Description
CAP FOR TEST TUBE 12*75MM PP, PACK OF 1000
Primary DI / UDI-DI
00810100050559
FDA product code
LXG
GMDN term
Test tube/reservoir cap
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Test tube/reservoir cap

Other devices from KB Medical (group), Inc.

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    Class II

  • Kbmed SN1B-2125

    Class II

  • Kbmed ES3

    Class II

  • Kbmed SBCN23-1H

    Class II

See all devices from KB Medical (group), Inc. →

Properties

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