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ASAHI PTCA Guide Wire PROWATER
EUDAMEDFDA UDIClass III (EU MDR)
Ref AGH146000Ref AGH146000J
Identity
- Trade Name
- ASAHI PTCA Guide Wire PROWATER EUDAMEDASAHI PTCA GUIDE WIRE ASAHI PROWATER 180cm J EUDAMEDPROWATER FDA UDI
- Generic Name
- Cardiac/peripheral vascular guidewire, single-use FDA UDI
- Device Name
- ASAHI PTCA GUIDE WIRE, ASAHI PTCA Guide Wire EUDAMED
- Model / Reference
- AGH146000 EUDAMEDAGH146000J EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 04547327085366 EUDAMED04547327056182 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04547327085366 EUDAMEDB-04547327056182 EUDAMED
- FDA Product Code
- DQX FDA UDI
- EMDN Code
- C04030201 INTERVENTIONAL CORONARY AND PERIPHERAL VASCULAR GUIDE WIRES, HYDROPHILIC EUDAMED
- GMDN Term
- Cardiac/peripheral vascular guidewire, single-use FDA UDI
Classification
- Device Class
- Class III EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1330 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
- Length — 180 Centimeter FDA UDIOuter Diameter — 0.014 Inch FDA UDI
ASAHI PTCA Guide Wire PROWATER by Asahi Intecc Co., Ltd. — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04547327085366 | Class III | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Asahi Intecc Co., Ltd.
- EUDAMED SRN
- JP-MF-000010199
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (3)
- EUDAMED 2a1f34db-0739-434d-a976-c35e972dbf89 61 fields · synced Aug 2, 2026
- EUDAMED e901a6ee-3d1a-42a9-b0de-13f4def06a20 61 fields · synced May 19, 2026
- FDA UDI 87f592b5-d367-4d7f-8ef9-39c8f95c5af8 33 fields · synced May 30, 2026