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TRACOE® comfort

FDA UDI

Class II (US FDA UDI)

by Tracoe medical GmbH

Identity

Trade Name
TRACOE® comfort FDA UDI
Generic Name
Tracheostomy tube, non-reinforced, non-customized, single-use FDA UDI
Device Name
Tube, with Swivel Speaking Valve, Type B,with additional oxygen supply port and with additional Inner cannula with 15 mm Connector FDA UDI
Model / Reference
REF 888-104-07A-N-O FDA UDI
Description
Tube, with Swivel Speaking Valve, Type B,with additional oxygen supply port and with additional Inner cannula with 15 mm Connector FDA UDI

Identifiers

Primary DI / UDI-DI
04035324022168 FDA UDI
510(k) Number
K781729 FDA UDI
FDA Product Code
BTO 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
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

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 — 5.8 Millimeter FDA UDI

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

Cleared under the same submission

K781729 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tracoe medical GmbH

Sources (1)

  • FDA UDI ea7ec2d6-dc35-4fd4-b56f-f9915da60384 38 fields · synced May 31, 2026