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COAPTIUM® Selector NCOSE0001

by Tissium SA

COAPTIUM® Selector NCOSE0001 is a Class I device made by Tissium SA, listed in FDA GUDID since 3 Oct 2025 (UDI-DI 03760279380377), 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 Number03760279380377 UDI-DI Date3 Oct 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  • Withdrawn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
COAPTIUM® Selector
Generic name
Medical ruler, single-use
Model / Ref / Catalog
NCOSE0001
Primary DI / UDI-DI
03760279380377
FDA product code
HAO
GMDN term
Medical ruler, single-use
Device class
Class I
Regulation number
882.4535
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HAO (Instrument, Surgical, Non-Powered).

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)