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Drill Bit, Ø3.2 Jacobs (FF-110-02)
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref FF-PSG-0007-00
Identity
- Trade Name
- Drill Bit, Ø3.2 Jacobs (FF-110-02) EUDAMEDFIREFLY® FDA UDI
- Generic Name
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
- Device Name
- FIREFLY - Pedicle Screw Guide EUDAMEDDrill Bit FDA UDI
- Model / Reference
- FF-PSG-0007-00 EUDAMEDFF-110-02 FDA UDI
- Description
- Drill Bit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851662007094 EUDAMEDFDA UDI
- Basic UDI-DI
- 0851662007FF-PSGTW EUDAMED
- Direct Marketing DI
- 00851662007094 EUDAMED
- FDA Product Code
- MNI FDA UDIPQC FDA UDI
- EMDN Code
- P090780 SPINAL PROSTHESES AND STABILISATION SYSTEMS - ACCESSORIES EUDAMED
- GMDN Term
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3070 FDA UDI
- Market of Registration
- Slovenia EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Drill Bit, Ø3.2 Jacobs (FF-110-02) by Mighty Oak Medical — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0851662007FF-PSGTW | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Mighty Oak Medical
- EUDAMED SRN
- US-MF-000039584
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED b38ca2bc-d472-4bd1-a5fa-38b03f760265 61 fields · synced Oct 10, 2026
- FDA UDI aeb1912c-391d-4253-b881-1f5ba2df390f 34 fields · synced May 30, 2026