Identity
- Trade Name
- FUBUKI XF FDA UDI
- Generic Name
- Vascular guide-catheter, single-use FDA UDI
- Model / Reference
- FBKX-8A80DY FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04547327142731 FDA UDI
- FDA Product Code
- QJP FDA UDIDQY FDA UDI
- GMDN Term
- Vascular guide-catheter, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1250 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
Dimensions & Sizes
- Size
- Catheter Gauge — 6 French FDA UDILength — 80 Centimeter FDA UDI
Category: Vascular guide-catheter, single-use
Fubuki Xf by Asahi Intecc Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Mach1™ — Boston Scientific · Class II
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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
- Asahi Intecc Co., Ltd.
Sources (1)
- FDA UDI 8ba335c0-5a12-49bd-b483-6c667c990c9d 33 fields · synced Jun 8, 2026