Identity
- Trade Name
- Ventlab FDA UDI
- Generic Name
- Atomizer, non-ventilatory FDA UDI
- Device Name
- Neb w/ Adult Aerosol Mask, 7' O2 Tube FDA UDI
- Model / Reference
- 5110 FDA UDI
- Description
- Neb w/ Adult Aerosol Mask, 7' O2 Tube FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10889483081907 FDA UDI
- FDA Product Code
- CAF FDA UDI
- GMDN Term
- Atomizer, non-ventilatory FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5630 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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 7 Feet FDA UDI
Category: Atomizer, non-ventilatory
Ventlab by Ventlab Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Atomizer, non-ventilatory.
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- LMA ATOMIZATION — TELEFLEX INCORPORATED · Class I
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- LMA ATOMIZATION — TELEFLEX INCORPORATED · Class I
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
- Ventlab Corp.
Sources (1)
- FDA UDI 3ab9128e-a842-461b-a628-96831fc4753f 36 fields · synced May 30, 2026