Identity
- Trade Name
- Sutter FDA UDI
- Generic Name
- Electrosurgical cable adaptor FDA UDI
- Device Name
- FlexTip RF Probe Adapter, Elliquence FDA UDI
- Model / Reference
- AR-S9805-010-E FDA UDI
- Description
- FlexTip RF Probe Adapter, Elliquence FDA UDI
Identifiers
- Catalog Number
- AR-S9805-010-E FDA UDI
- Primary DI / UDI-DI
- ESUMARS9805010E0 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Electrosurgical cable adaptor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: Electrosurgical cable adaptor
Sutter by Sutter Medizintechnik GmbH — 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
- Sutter Medizintechnik GmbH
Sources (1)
- FDA UDI 0c51217a-3987-47ec-978a-aee91efaff78 35 fields · synced Jun 1, 2026