Identity
- Trade Name
- JETSTREAM™ PVCN100 FDA UDI
- Generic Name
- General-purpose suction system, line-powered FDA UDI
- Device Name
- Console FDA UDI
- Model / Reference
- 050599-001R FDA UDI
- Description
- Console FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08714729890454 FDA UDI
- FDA Product Code
- MCW FDA UDI
- GMDN Term
- General-purpose suction system, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4875 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: General-purpose suction system, line-powered
Jetstream™ Pvcn100 by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as General-purpose suction system, line-powered.
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- ANGIOJET — Bayer Healthcare · Class III
- Winx® — Apnicure, Inc. · Class II
- Winx® — Apnicure, Inc. · 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
- Boston Scientific
Sources (1)
- FDA UDI 68268c3c-fbe5-465d-ab37-443581463c74 33 fields · synced May 30, 2026