FDA UDI In Commercial Distribution 🇺🇸 United States

Gibralt

DI: 10885862233486 · Model: 05-004-00-2230 · Choice Spine, LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Gibralt
Primary DI
10885862233486
Version / Model
05-004-00-2230
Catalog Number
05-004-00-2230
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
bb2c9edc-d22f-4299-b802-f202023b975f

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

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

Identifiers

Type ID
Primary 10885862233486

Device Sizes

Type Value Unit Text
Device Size Text, specify 22mm - 30mm length