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Temno® 10884450444624

by Merit Medical Systems, Inc.

Temno® 10884450444624 (T2011/B) is a Class II device made by Merit Medical Systems, Inc., listed in FDA GUDID since 12 Jun 2020 (UDI-DI 10884450444624), 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 Number10884450444624 UDI-DI Date12 Jun 2020ListedStatusListed 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  • Withdrawn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
Temno®
Generic name
Soft-tissue biopsy procedure kit, non-medicated
Model / Ref / Catalog
10884450444624, T2011/B
Primary DI / UDI-DI
10884450444624
FDA product code
FCG
GMDN term
Soft-tissue biopsy procedure kit, non-medicated
Device class
Class II
Regulation number
876.1075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Soft-tissue biopsy procedure kit, non-medicated

Similar devices in this category

Other devices filed under Soft-tissue biopsy procedure kit, non-medicated.

Other devices from Merit Medical Systems, Inc.

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Properties

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