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Azure 17.044

by Terrats Medical SL

Azure 17.044 (ARNAC-ICD35) is a Class I device made by Terrats Medical SL, listed in FDA GUDID since 25 Jun 2024 (UDI-DI 08435457299738), 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 Number08435457299738 UDI-DI Date25 Jun 2024ListedStatusListed 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  • Withdrawn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 implant abutment analog, laboratory
Model / Ref / Catalog
17.044, ARNAC-ICD35
Primary DI / UDI-DI
08435457299738
FDA product code
NDP
GMDN term
Dental implant abutment analog, laboratory
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 implant abutment analog, laboratory

Similar devices

Other devices filed under FDA product code NDP (Accessories, implant, dental, endosseous).

Other devices from Terrats Medical, S.L.

See all devices from Terrats Medical, S.L. →

Properties

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