← Back to catalogue

TRACOE silcosoft

FDA UDI

Class II (US FDA UDI)

by Tracoe medical GmbH

Identity

Trade Name
TRACOE silcosoft FDA UDI
Generic Name
Tracheostomy tube, non-reinforced, non-customized, single-use FDA UDI
Device Name
Tracheostomy Tube for Children FDA UDI
Model / Reference
REF 370-3.0-C55 FDA UDI
Description
Tracheostomy Tube for Children FDA UDI

Identifiers

Catalog Number
REF 370-3.0-C55 FDA UDI
Primary DI / UDI-DI
04035324029204 FDA UDI
510(k) Number
K172720 FDA UDI
FDA Product Code
JOH FDA UDI
GMDN Term
Tracheostomy tube, non-reinforced, non-customized, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 3.0 Millimeter FDA UDI

Category: Tracheostomy tube, non-reinforced, non-customized, single-use

TRACOE silcosoft by Tracoe medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy tube, non-reinforced, non-customized, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tracoe medical GmbH

Sources (1)

  • FDA UDI e42506f4-24b8-4ca9-be08-9970a041e522 38 fields · synced Jun 1, 2026