FDA UDI In Commercial Distribution 🇺🇸 United States

Idys®-LLIF

DI: 03700780635078 · Model: 45720000 · CLARIANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Idys®-LLIF
Primary DI
03700780635078
Version / Model
45720000
Catalog Number
45720000
Company Name
CLARIANCE
Labeler DUNS
296568400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-07
Public Version
1
Public Version Date
2021-07-15
Public Version Status
New
Public Device Record Key
65c63579-bf5f-4804-ae7a-cf6dd389adad

Device Description

TIGHTENING WRENCH

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

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

Identifiers

Type ID
Primary 03700780635078

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K202032 000