Identity
- Trade Name
- PROWLER FDA UDI
- Generic Name
- Vascular microcatheter FDA UDI
- Device Name
- PROWLER EX Microcatheter Tip Markers: 2 2.3F (0.75 mm) (0.95 mm) .021 Inch (0.5 mm) 5cm 160cm 3 cm Contents: 1 Microcatheter and 1 Shape Mandrel FDA UDI
- Model / Reference
- MC2165S2U FDA UDI
- Description
- PROWLER EX Microcatheter Tip Markers: 2 2.3F (0.75 mm) (0.95 mm) .021 Inch (0.5 mm) 5cm 160cm 3 cm Contents: 1 Microcatheter and 1 Shape Mandrel FDA UDI
Identifiers
- Catalog Number
- MC2165S2U FDA UDI
- Primary DI / UDI-DI
- 10886704084693 FDA UDI
- FDA Product Code
- DQY FDA UDIKRA FDA UDIQJP FDA UDI
- GMDN Term
- Vascular microcatheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1250 FDA UDI870.1210 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Vascular microcatheter
Prowler by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Medos International Sàrl
Sources (1)
- FDA UDI bbc83128-559c-40db-8ceb-24127183dcdb 36 fields · synced Jun 8, 2026