FDA UDI In Commercial Distribution 🇺🇸 United States

Idys™- TLIF

DI: 03700780613311 · Model: 06714507 · CLARIANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Idys™- TLIF
Primary DI
03700780613311
Version / Model
06714507
Catalog Number
06714507
Company Name
CLARIANCE
Labeler DUNS
296568400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-22
Public Version
1
Public Version Date
2018-06-22
Public Version Status
New
Public Device Record Key
3bb6d735-c921-4b51-813f-66b053c05b0c

Device Description

FANTÔME TLIF

Device Characteristics

Single Use
No
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
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

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 03700780613311

Customer Contacts

Phone
7738687041

Device Sizes

Type Value Unit Text
Length 33 Millimeter
Height 7 Millimeter