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TRACOE care REF 910-A

by Tracoe medical GmbH

TRACOE care REF 910-A is a Class I device made by Tracoe medical GmbH, listed in FDA GUDID since 24 Oct 2015 (UDI-DI 04035324061211), 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 Number04035324061211 UDI-DI Date24 Oct 2015ListedStatusListed 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  • Withdrawn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
TRACOE care
Generic name
Tracheostomy tube dressing
Model / Ref / Catalog
REF 910-A
Primary DI / UDI-DI
04035324061211
FDA product code
NAD
GMDN term
Tracheostomy tube dressing
Device class
Class I
Regulation number
878.4020
GUDID distribution status
In Commercial Distribution
Size
Length — 9.8 Centimeter
Width — 9.0 Centimeter

Similar devices

Other devices filed under FDA product code NAD (Dressing,wound,occlusive).

Other devices from Tracoe medical GmbH

See all devices from Tracoe medical GmbH →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)