FDA UDI In Commercial Distribution 🇺🇸 United States

Idys™- PLIF

DI: 03700780602124 · Model: 04714312 · CLARIANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Idys™- PLIF
Primary DI
03700780602124
Version / Model
04714312
Catalog Number
04714312
Company Name
CLARIANCE
Labeler DUNS
296568400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-21
Public Version
1
Public Version Date
2018-06-21
Public Version Status
New
Public Device Record Key
762f122e-a6fa-446f-8253-41525e0889ae

Device Description

PLIF TRIAL

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 03700780602124

Customer Contacts

Phone
7738687041

Device Sizes

Type Value Unit Text
Length 25 Millimeter
Height 12 Millimeter