Identity
- Trade Name
- Vapotherm FDA UDI
- Generic Name
- Negative-pressure face tent FDA UDI
- Device Name
- Felix-1, India Version FDA UDI
- Model / Reference
- FELIX-1-IN FDA UDI
- Description
- Felix-1, India Version FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00841737104384 FDA UDI
- FDA Product Code
- CBD FDA UDI
- GMDN Term
- Negative-pressure face tent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Negative-pressure face tent
Vapotherm by Vapotherm Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Negative-pressure face tent.
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
- Vapotherm Inc.
Sources (1)
- FDA UDI 3a860e21-6201-487c-90a3-f51e1a1c28fc 33 fields · synced Jun 8, 2026