FDA UDI In Commercial Distribution 🇺🇸 United States

Galaxy

DI: 08809263396415 · Model: A · DIOMEDICAL CO.,LTD.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Galaxy
Primary DI
08809263396415
Version / Model
A
Catalog Number
NP1081124
Company Name
DIOMEDICAL CO.,LTD.
Labeler DUNS
557795909
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b42332ff-693a-48cf-a0e0-e0fe98ff895a

Device Description

Galaxy PLIF cage H10 x W11 x L24 x A8

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 08809263396415

Customer Contacts

Phone
+82313699470 ext. 112

Premarket Submissions

Submission Number Supplement Number
K122872 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Width 11mm, Length 24mm, Angle 8
Height 10 Millimeter