Identity
- Trade Name
- Sutter FDA UDI
- Generic Name
- Surgical irrigation pump FDA UDI
- Device Name
- CURIS® RF Generator interconnecting cable FDA UDI
- Model / Reference
- 93008120 FDA UDI
- Description
- CURIS® RF Generator interconnecting cable FDA UDI
Identifiers
- Catalog Number
- 93008120 FDA UDI
- Primary DI / UDI-DI
- ESUM930081200 FDA UDI
- FDA Product Code
- FQH FDA UDI
- GMDN Term
- Surgical irrigation pump FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5475 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
Yes
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: Surgical irrigation pump
Sutter by Sutter Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Wellead Portable Roller Irrigation Pump — Well Lead Medical Co., Ltd · 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
- Sutter Medizintechnik GmbH
Sources (1)
- FDA UDI 1cdf05af-4f56-4cca-b926-7e01209ffcbe 35 fields · synced May 30, 2026