Identity
- Trade Name
- Vacuum Pump Tubing FDA UDI
- Generic Name
- Disposable vacuum tubing FDA UDI
- Model / Reference
- 17201 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07350025915647 FDA UDI
- FDA Product Code
- GAZ FDA UDI
- GMDN Term
- Disposable vacuum tubing 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
Yes
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: Disposable vacuum tubing
Vacuum Pump Tubing by Vitrolife Sweden AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Disposable vacuum tubing.
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- KAMVAC — DEPUY ORTHOPAEDICS, INC. · Class II
- KAMVAC — DEPUY ORTHOPAEDICS, INC. · Class II
- Tube set for suction, single-use — W.O.M. World of Medicine GmbH · Class II
- Prabadin — Prabadin Corp · Class II
- PLEUR-EVAC — TELEFLEX 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 II | Pending data |
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Manufacturer
- Manufacturer
- Vitrolife Sweden AB
Sources (1)
- FDA UDI 7756cb28-5a38-4930-ac23-3cd786689bef 32 fields · synced Jun 8, 2026