Identity
- Trade Name
- INTER-THERM HMEF - STERILE FDA UDI
- Generic Name
- Heat/moisture exchanger/microbial filter, sterile FDA UDI
- Device Name
- INTER-THERM HMEF - STERILE FDA UDI
- Model / Reference
- 1341007S FDA UDI
- Description
- INTER-THERM HMEF - STERILE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05030267052172 FDA UDI
- 510(k) Number
- K092451 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 - Sterile by Intersurgical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Heat/moisture exchanger/microbial filter, sterile.
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Cleared under the same submission
K092451 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Intersurgical Incorporated
Sources (1)
- FDA UDI 63afb27e-1c18-424c-b8f4-e6b2c0d35756 35 fields · synced Jun 1, 2026