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Resp-O2 Heat Moisture Exchanger and B/V Filter (HMEF) 1000, CO2 Por
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Resp-O2 Heat Moisture Exchanger and B/V Filter (HMEF) 1000, CO2 Por FDA UDI
- Generic Name
- Heat/moisture exchanger/microbial medical gas filter FDA UDI
- Device Name
- Adult,Tidal Volume Rage (150-1000 mL), Media (Foam + Flat Media), Dead Space (70 mL), Breathing Resistance (1.9 cm H2O at 60 L / min, Weight (24.5g) FDA UDI
- Model / Reference
- 30100 FDA UDI
- Description
- Adult,Tidal Volume Rage (150-1000 mL), Media (Foam + Flat Media), Dead Space (70 mL), Breathing Resistance (1.9 cm H2O at 60 L / min, Weight (24.5g) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840117305656 FDA UDI
- FDA Product Code
- CAH FDA UDI
- GMDN Term
- Heat/moisture exchanger/microbial medical gas filter 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Heat/moisture exchanger/microbial medical gas filter
Resp-O2 Heat Moisture Exchanger and B/V Filter (HMEF) 1000, CO2 Por by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Dynarex Corp.
Sources (1)
- FDA UDI b23b0188-4b14-4385-9a14-9fb5af6050e5 33 fields · synced Jun 1, 2026