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Azure DTC24H175

by Terrats Medical SL

Azure DTC24H175 (ARA-DTC24H175) is a Class I device made by Terrats Medical SL, listed in FDA GUDID since 8 Sep 2023 (UDI-DI 08435457285595), 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 Number08435457285595 UDI-DI Date8 Sep 2023ListedStatusListed 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  • Withdrawn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
Azure
Generic name
Dental torque wrench
Model / Ref / Catalog
DTC24H175, ARA-DTC24H175
Primary DI / UDI-DI
08435457285595
FDA product code
NDP
GMDN term
Dental torque wrench
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental torque wrench

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Other devices filed under Dental torque wrench.

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Properties

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