FDA UDI In Commercial Distribution 🇺🇸 United States

Idys™- C

DI: 03700780628476 · Model: 05714405 · CLARIANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Idys™- C
Primary DI
03700780628476
Version / Model
05714405
Catalog Number
05714405
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
7fe5b106-cdf0-485c-8a1d-8a731cdcf5a6

Device Description

FIXED 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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

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

Identifiers

Type ID
Primary 03700780628476

Customer Contacts

Phone
7738687041

Device Sizes

Type Value Unit Text
Height 5 Millimeter
Width 14 Millimeter
Depth 13 Millimeter