← Back to catalogue

Fixation Screw (FF-105-50)

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref FF-PSG-0007-00

by Mighty Oak Medical

Identity

Trade Name
Fixation Screw (FF-105-50) EUDAMED
FIREFLY® FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
FIREFLY - Pedicle Screw Guide EUDAMED
Fixation Screw FDA UDI
Model / Reference
FF-PSG-0007-00 EUDAMED
FF-105-50 FDA UDI
Description
Fixation Screw FDA UDI

Identifiers

Primary DI / UDI-DI
00851662007056 EUDAMEDFDA UDI
Basic UDI-DI
0851662007FF-PSGTW EUDAMED
Direct Marketing DI
00851662007056 EUDAMED
FDA Product Code
MNI FDA UDI
PQC FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Fixation Screw (FF-105-50) 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Mighty Oak Medical
EUDAMED SRN
US-MF-000039584
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED d6a8fc75-338b-4f58-83e0-2d2d5a9e8356 61 fields · synced Oct 8, 2026
  • FDA UDI 67701c63-ac4c-4237-b6c8-5c66b8b6f82d 34 fields · synced May 30, 2026