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TRACOE modular

FDA UDI

Class I (US FDA UDI)

by Tracoe medical GmbH

Identity

Trade Name
TRACOE modular FDA UDI
Generic Name
Heat/moisture exchanger, single-use FDA UDI
Device Name
TRACOE humid assist IV, 30 units FDA UDI
Model / Reference
REF 642 FDA UDI
Description
TRACOE humid assist IV, 30 units FDA UDI

Identifiers

Catalog Number
REF 642 FDA UDI
Primary DI / UDI-DI
04035324016952 FDA UDI
FDA Product Code
BYD FDA UDI
GMDN Term
Heat/moisture exchanger, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5375 FDA UDI
Commercial Distribution
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

Category: Heat/moisture exchanger, single-use

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

Similar devices

Also classified as Heat/moisture exchanger, single-use.

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 ab4a9a2c-65bc-437c-98bd-90f3906c3aa5 37 fields · synced May 31, 2026