Hermes PTA Balloon Dilatation Catheter
EUDAMEDFDA UDIClass IIa (EU MDR)
Identity
- Trade Name
- Hermes EUDAMEDHermes NC PTA Balloon Dilatation Catheter FDA UDI
- Generic Name
- Peripheral angioplasty balloon catheter, basic FDA UDI
- Device Name
- Hermes PTA Balloon Dilatation Catheter EUDAMED
- Model / Reference
- 820-080100-070 EUDAMEDrev 01 FDA UDI
Identifiers
- Catalog Number
- 820-080100-070U FDA UDI
- Primary DI / UDI-DI
- 06958481449419 EUDAMEDFDA UDI
- Basic UDI-DI
- B-06958481449419 EUDAMED695848140016M6 EUDAMED
- FDA Product Code
- LIT FDA UDI
- EMDN Code
- C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED
- GMDN Term
- Peripheral angioplasty balloon catheter, basic FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1250 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
No
Category: Peripheral angioplasty balloon catheter, basic
Hermes PTA Balloon Dilatation Catheter by BrosMed Medical Co., Ltd. — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID
Similar devices
Also classified as Peripheral angioplasty balloon catheter, basic.
- Advocate™ — Merit Medical Systems, Inc. · Class II
- Senri — KANEKA Corporation · Class IIa
- Jade PTA Balloon Dilatation Catheter — OrbusNeich Medical (ShenZhen) Co., Ltd. · Class II
- ZENFluxion — Zylox-Tonbridge Medical Technology Co., Ltd. · Class III
- Pacific™ Plus — MEDTRONIC, INC. · Class II
- Metacross OTW — KANEKA Corporation · Class IIa
- Armada — Abbott Vascular · Class II
- RapidCross — Covidien LP · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
CE/MDD
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-06958481449419 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-06958481449419 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- BrosMed Medical Co., Ltd
- EUDAMED SRN
- CN-MF-000007501
- Authorised Representative
- Brosmed Medical B.V. NL-AR-000002616
Sources (3)
- EUDAMED b2864176-e1bd-4c9e-964b-8ec2cd6134c0 61 fields · synced Jun 20, 2026
- EUDAMED 8b35ea48-640a-4684-86e9-df9829547920 61 fields · synced May 18, 2026
- FDA UDI c9bcef83-2c27-430b-b869-13072780dda4 33 fields · synced May 30, 2026