Identity
- Trade Name
- Branchor X FDA UDI
- Generic Name
- Intravascular occluding balloon catheter, image-guided FDA UDI
- Model / Reference
- BBG890-XSW FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04547327154109 FDA UDI
- FDA Product Code
- QJP FDA UDI
- GMDN Term
- Intravascular occluding balloon catheter, image-guided 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 — 8 French FDA UDILength — 90 Centimeter FDA UDI
Category: Intravascular occluding balloon catheter, image-guided
Branchor X by Asahi Intecc Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intravascular occluding balloon catheter, image-guided.
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- Pennig Minifixator — Orthofix, Inc. · Class II
- LMI BILUMEN IRRIGATION ARTERIAL EMBOLECTOMY CATHETER — LUCAS MEDICAL INC · Class II
- HyperFormTM — Micro Therapeutics, Inc. · Class II
- CELLO™, Balloon Guide Catheter — Fuji Systems Corp. · 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
- Asahi Intecc Co., Ltd.
Sources (1)
- FDA UDI 442a1de4-afdf-4fa3-a827-057192a0ff28 33 fields · synced May 31, 2026