Identity
- Trade Name
- DIATHERMY BIPOLAR CABLE FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reusable FDA UDI
- Device Name
- This re-usable device is an accessory for ZEISS phaco systems. It has been designed to connect the diathermy handpieces to the main device during human eye surgery. FDA UDI
- Model / Reference
- 303060-0250-000 FDA UDI
- Description
- This re-usable device is an accessory for ZEISS phaco systems. It has been designed to connect the diathermy handpieces to the main device during human eye surgery. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04049539100498 FDA UDI
- FDA Product Code
- HQR FDA UDI
- GMDN Term
- Electrical-only medical device connection cable, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Electrical-only medical device connection cable, reusable
Diathermy Bipolar Cable by Carl Zeiss Meditec AG — 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
- Carl Zeiss Meditec AG
Sources (1)
- FDA UDI 385d90d6-30ed-4071-bbf5-2652ac4249e1 33 fields · synced Jun 8, 2026