FDA UDI In Commercial Distribution 🇺🇸 United States

KIT BONE GRAFT

DI: 07899995209283 · Model: KENX · Sin Sistema de Implante Nacional S/A
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KIT BONE GRAFT
Primary DI
07899995209283
Version / Model
KENX
Catalog Number
KENX
Company Name
Sin Sistema de Implante Nacional S/A
Labeler DUNS
904569092
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-27
Public Version
1
Public Version Date
2023-11-06
Public Version Status
New
Public Device Record Key
d7a148f2-fb26-40ea-ba38-42eed6ebb4ac

Device Description

KIT BONE GRAFT

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

GMDN Terms

Code Name
45147 Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 07899995209283

Premarket Submissions

Submission Number Supplement Number
K222005 000