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COAPTIUM® Connect NCOCO3075

by Tissium SA

COAPTIUM® Connect NCOCO3075 is a Class II device made by Tissium SA, listed in FDA GUDID since 22 Sep 2025 (UDI-DI 03760279380131), 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 Number03760279380131 UDI-DI Date22 Sep 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  • Withdrawn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® Connect
Generic name
Nerve guide, synthetic polymer, bioabsorbable
Model / Ref / Catalog
NCOCO3075
Primary DI / UDI-DI
03760279380131
FDA product code
SFD
GMDN term
Nerve guide, synthetic polymer, bioabsorbable
Device class
Class II
Regulation number
882.5270
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Outer Diameter — 3.0 Millimeter
Length — 7.5 Millimeter

Related devices

Category: Nerve guide, synthetic polymer, bioabsorbable

Other devices from Tissium SA

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Properties

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