Identity
- Trade Name
- DrillCut-X FDA UDI
- Generic Name
- Tissue morcellation system FDA UDI
- Device Name
- DrillCut-X® II Shaver Handpiece FDA UDI
- Model / Reference
- 40712050 FDA UDI
- Description
- DrillCut-X® II Shaver Handpiece FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04048551253632 FDA UDI
- FDA Product Code
- ERL FDA UDI
- GMDN Term
- Tissue morcellation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.4250 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Tissue morcellation system
DrillCut-X by Karl Storz GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Tissue morcellation system.
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- Versacut Tissue Morcellator — Lumenis · Class II
- BLUEENDO — TROKAMED GmbH · Class II
- Versacut™ — Lumenis · 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
- Karl Storz GmbH & Co. KG
Sources (1)
- FDA UDI 17c27aeb-a7d2-4b5b-aa25-4bf6a6f14522 33 fields · synced Jun 1, 2026