Identity
- Trade Name
- HME DigiTop O2 FDA UDI
- Generic Name
- Tracheostoma protective filter FDA UDI
- Device Name
- The HME DigiTop O2 is an accessory to Freevent HMEs and Provox FreeHands HME's. For patients spontaneously breathing through a tracheostoma and having a need of extra oxygen. FDA UDI
- Model / Reference
- 7756 FDA UDI
- Description
- The HME DigiTop O2 is an accessory to Freevent HMEs and Provox FreeHands HME's. For patients spontaneously breathing through a tracheostoma and having a need of extra oxygen. FDA UDI
Identifiers
- Catalog Number
- 7756 FDA UDI
- Primary DI / UDI-DI
- 07331791008320 FDA UDI
- FDA Product Code
- BYD FDA UDI
- GMDN Term
- Tracheostoma protective filter 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
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
Yes
FDA UDI
Category: Tracheostoma protective filter
HME DigiTop O2 by Atos Medical Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Atos Medical Inc.
Sources (1)
- FDA UDI 4a3dab02-1948-4c36-877d-592e879535ac 36 fields · synced May 31, 2026