Identity
- Trade Name
- Connecting Tube for Manujet III FDA UDI
- Generic Name
- Manual jet ventilation device FDA UDI
- Device Name
- n/a FDA UDI
- Model / Reference
- 54-05-111 FDA UDI
- Description
- n/a FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04250105604283 FDA UDI
- FDA Product Code
- BZO FDA UDI
- GMDN Term
- Manual jet ventilation device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5975 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
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 100 Centimeter FDA UDI
Category: Manual jet ventilation device
Connecting Tube for Manujet III by VBM Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Manual jet ventilation device.
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- Ventrain — Ventinova Medical B.V. · Class II
- Manual Jet Ventilator — INSTRUMENTATION INDUSTRIES, INCORPORATED · Class II
- Manual Jet Ventilator — INSTRUMENTATION INDUSTRIES, INCORPORATED · Class II
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
- VBM Medizintechnik GmbH
Sources (1)
- FDA UDI 35d15345-e85f-45ec-b637-478c17842ae5 36 fields · synced May 30, 2026