FDA UDI In Commercial Distribution 🇺🇸 United States

SpaceVision® PLIF

DI: 03663136029344 · Model: SPL1-C12-29-00 · SPINEVISION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SpaceVision® PLIF
Primary DI
03663136029344
Version / Model
SPL1-C12-29-00
Company Name
SPINEVISION
Labeler DUNS
390377518
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-20
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
ead8313a-e1e4-4420-a49e-a1247e9d0a0a

Device Description

Sterile PLIF cage H12-L29-A00

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 03663136029344

Customer Contacts

Phone
+33153332525

Device Sizes

Type Value Unit Text
Length 29 Millimeter
Height 12 Millimeter