← Back to catalogue

Galaxy Fixation Gemini

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
GALAXY FIXATION GEMINI FDA UDI
Generic Name
External orthopaedic fixation system, single-use FDA UDI
Device Name
GALAXY FIXATION GEMINI PELVIS SET COMPLETE STERILE FDA UDI
Model / Reference
1 FDA UDI
Description
GALAXY FIXATION GEMINI PELVIS SET COMPLETE STERILE FDA UDI

Identifiers

Catalog Number
99-94710 FDA UDI
Primary DI / UDI-DI
18053340348805 FDA UDI
510(k) Number
K113770 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
External orthopaedic fixation system, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: External orthopaedic fixation system, single-use

Galaxy Fixation Gemini by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External orthopaedic fixation system, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Orthofix, Inc.

Sources (1)

  • FDA UDI 03c98ed3-77bf-4418-b1ff-7d0947636230 36 fields · synced May 31, 2026