Identity
- Trade Name
- Ventlab FDA UDI
- Generic Name
- Anaesthesia face mask, single-use FDA UDI
- Device Name
- MASK CLEAR CUSHION DISP LARGE ADULT SZ 5 BLUE FDA UDI
- Model / Reference
- 4-0110-05 FDA UDI
- Description
- MASK CLEAR CUSHION DISP LARGE ADULT SZ 5 BLUE FDA UDI
Identifiers
- Catalog Number
- 4-0110-05 FDA UDI
- Primary DI / UDI-DI
- 10889483039625 FDA UDI
- FDA Product Code
- BSJ FDA UDI
- GMDN Term
- Anaesthesia face mask, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5550 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 50 Milliliter FDA UDI
Ventlab by Ventlab Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Ventlab Corp.
Sources (1)
- FDA UDI 3d3e49d1-c051-4316-8c45-b0723a425dbe 37 fields · synced Jun 8, 2026