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Universal Chuck Set for the IntelliSense Drill System
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Universal Chuck Set for the IntelliSense Drill System FDA UDI
- Generic Name
- Surgical drill chuck key FDA UDI
- Device Name
- Universal Key to the keyed chuck for IntelliSense Drill FDA UDI
- Model / Reference
- 1.0 FDA UDI
- Description
- Universal Key to the keyed chuck for IntelliSense Drill FDA UDI
Identifiers
- Catalog Number
- MCG8007 FDA UDI
- Primary DI / UDI-DI
- B666MCG80070 FDA UDI
- FDA Product Code
- HWE FDA UDI
- GMDN Term
- Surgical drill chuck key FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
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: Surgical drill chuck key
Universal Chuck Set for the IntelliSense Drill System by Mcginley Orthopaedic Innovations, Inc — Class I — FDA UDI — listed in FDA GUDID
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- De Soutter Medical — De Soutter Medical, Ltd. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Mcginley Orthopaedic Innovations, Inc
Sources (1)
- FDA UDI c94d7f15-712c-482e-87ee-20d4c410f6aa 35 fields · synced Jun 8, 2026