TRACOE silcosoft REF 371-2.5-C40

by Tracoe medical GmbH

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04035324029709 UDI-DI	Date24 May 2018Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: TRACOE silcosoft
Generic Name: Tracheostomy tube, non-reinforced, non-customized, single-use
Model / Ref / Catalog: REF 371-2.5-C40

Primary DI / UDI-DI: 04035324029709
510(k) Number: K172720
FDA Product Code: JOH
GMDN Term: Tracheostomy tube, non-reinforced, non-customized, single-use

Device Class: Class II
Regulation Number: 868.5800
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Conditional

Size: Lumen/Inner Diameter — 2.5 Millimeter

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Properties

Sterile
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (10)

Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Manufacturing Date: No