Identity
- Trade Name
- i-Cut Power Supply Type A FDA UDI
- Generic Name
- Basic power supply, reusable FDA UDI
- Device Name
- The i-Cut system is indicated for morcellating and extracting tissue in laparoscopic, gynecologic surgical procedures. The i-Cut is electrically operated by a DC Motor which is powered by a 24V AC/DC mains adapter. The non-sterile i-Cut Power Supply with power cord is supplied separately to power the device. FDA UDI
- Model / Reference
- ICT5050 FDA UDI
- Description
- The i-Cut system is indicated for morcellating and extracting tissue in laparoscopic, gynecologic surgical procedures. The i-Cut is electrically operated by a DC Motor which is powered by a 24V AC/DC mains adapter. The non-sterile i-Cut Power Supply with power cord is supplied separately to power the device. FDA UDI
Identifiers
- Primary DI / UDI-DI
- EAMIICT50500 FDA UDI
- 510(k) Number
- K243821 FDA UDI
- FDA Product Code
- HET FDA UDI
- GMDN Term
- Basic power supply, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1720 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
Category: Basic power supply, reusable
i-Cut Power Supply Type A by AMI Agency for Medical Innovations GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Basic power supply, reusable.
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- QINFLOW AC STATION INTRO SET WARRIOR — QUALITY IN FLOW LTD · Class II
- SHIP KIT, POWER SUPPLY, LP35 — PHYSIO-CONTROL, Inc. · Class II
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- C-MAC — Karl Storz GmbH & Co. KG · Class I
Cleared under the same submission
K243821 also covers:
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- AMI Agency for Medical Innovations GmbH
Sources (2)
- FDA UDI 170b3b8a-677d-42f4-879a-2fff1c0f0415 35 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 2, 2026