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Inter-Therm Hmef With Luer Port - Sterile

FDA UDI

Class II (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
INTER-THERM HMEF WITH LUER PORT - STERILE FDA UDI
Generic Name
Heat/moisture exchanger/microbial filter, sterile FDA UDI
Device Name
INTER-THERM HMEF WITH LUER PORT - STERILE FDA UDI
Model / Reference
1341000S FDA UDI
Description
INTER-THERM HMEF WITH LUER PORT - STERILE FDA UDI

Identifiers

Primary DI / UDI-DI
05030267052165 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Heat/moisture exchanger/microbial filter, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 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

Yes

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

Yes

FDA UDI

Category: Heat/moisture exchanger/microbial filter, sterile

Inter-Therm Hmef With Luer Port - Sterile by Intersurgical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heat/moisture exchanger/microbial filter, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 45659a9d-31cd-46d1-a4db-79c1a049a519 34 fields · synced Jun 8, 2026