FDA UDI In Commercial Distribution 🇺🇸 United States

Galaxy II Surgical Retractor

DI: 15060557440423 · Model: GX10 · MOSAIC SURGICAL LIMITED
Product Codes
4
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Galaxy II Surgical Retractor
Primary DI
15060557440423
Version / Model
GX10
Company Name
MOSAIC SURGICAL LIMITED
Labeler DUNS
222357455
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2026-04-09
Public Version
1
Public Version Date
2026-04-17
Public Version Status
New
Public Device Record Key
ffb563fb-bacd-4096-829c-f0813889ffb5

Device Description

Galaxy II HandMe Frame

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KAL Retractor, Ent
HDL Retractor, Vaginal
FFO Retractor, Self-Retaining
GAD Retractor

GMDN Terms

Code Name
47822 Surgical retraction system mounting frame, single-use

Identifiers

Type ID
Unit of Use 05060557440426
Primary 15060557440423