FDA UDI In Commercial Distribution 🇺🇸 United States

Galaxy II Surgical Retractor

DI: 15060557440164 · Model: JUNEGX-2020 · MOSAIC SURGICAL LIMITED
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Galaxy II Surgical Retractor
Primary DI
15060557440164
Version / Model
JUNEGX-2020
Company Name
MOSAIC SURGICAL LIMITED
Labeler DUNS
222357455
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-26
Public Version
1
Public Version Date
2026-04-03
Public Version Status
New
Public Device Record Key
6648afbc-654c-40a4-8fc6-0fa5e0694de8

Device Description

Galaxy II Male Kit

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

GMDN Terms

Code Name
47820 Surgical retraction system, single-use

Identifiers

Type ID
Primary 15060557440164