FDA UDI In Commercial Distribution 🇺🇸 United States

Idys™- LIF

DI: 03700780600441 · Model: 06532912-S · CLARIANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Idys™- LIF
Primary DI
03700780600441
Version / Model
06532912-S
Catalog Number
06532912-S
Company Name
CLARIANCE
Labeler DUNS
296568400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
7060a91b-b4e8-4658-8eef-dc350b69c5a5

Device Description

TLIF CAGE

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
Yes
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 03700780600441

Customer Contacts

Phone
7738687041

Premarket Submissions

Submission Number Supplement Number
K131178 000

Device Sizes

Type Value Unit Text
Height 12 Millimeter
Depth 11 Millimeter
Width 29 Millimeter