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Inter-Therm T+ Hme

FDA UDI

Class I (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
INTER-THERM T+ HME FDA UDI
Generic Name
Heat/moisture exchanger, single-use FDA UDI
Device Name
INTER-THERM T+ HME FDA UDI
Model / Reference
1875000 FDA UDI
Description
INTER-THERM T+ HME FDA UDI

Identifiers

Primary DI / UDI-DI
05030267155903 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

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

Yes

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

Inter-Therm T+ Hme by Intersurgical Incorporated — 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
Intersurgical Incorporated

Sources (1)

  • FDA UDI 3c3e19c9-e8a7-4f5a-96dd-c804e22ac36f 34 fields · synced May 30, 2026