← Back to catalogue

TRACOE® larynx

FDA UDI

Class I (US FDA UDI)

by Tracoe medical GmbH

Identity

Trade Name
TRACOE® larynx FDA UDI
Generic Name
Tracheostoma button FDA UDI
Device Name
TRACOE grid button Long FDA UDI
Model / Reference
REF 603-06 FDA UDI
Description
TRACOE grid button Long FDA UDI

Identifiers

Primary DI / UDI-DI
04035324043415 FDA UDI
FDA Product Code
KAC FDA UDI
GMDN Term
Tracheostoma button FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 6.0 Millimeter FDA UDI

TRACOE® larynx by Tracoe medical GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 07f79297-1293-4fd9-ab8d-b8e7b754553a 37 fields · synced Jun 8, 2026