Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Multi-purpose surgical power tool system, line-powered FDA UDI
- Device Name
- MICROSPEED UNI MICRO 100 MOTOR FDA UDI
- Model / Reference
- GD679 FDA UDI
- Description
- MICROSPEED UNI MICRO 100 MOTOR FDA UDI
Identifiers
- Catalog Number
- GD679 FDA UDI
- Primary DI / UDI-DI
- 04038653369942 FDA UDI
- FDA Product Code
- HBC FDA UDI
- GMDN Term
- Multi-purpose surgical power tool system, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4360 FDA UDI
- Commercial Distribution
- Not 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
Aesculap by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Aesculap, Inc.
Sources (1)
- FDA UDI acdd02ae-2f97-4fd5-8828-356a023bf2c3 36 fields · synced Jun 1, 2026