FDA UDI In Commercial Distribution 🇺🇸 United States

CLS® Brevius® Kinectiv®

DI: 00889024280786 · Model: 01.00297.090 · Zimmer GmbH
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CLS® Brevius® Kinectiv®
Primary DI
00889024280786
Version / Model
01.00297.090
Company Name
Zimmer GmbH
Labeler DUNS
488133448
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-07
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
d532253e-1d77-4c98-9d56-1f60cb1ab7d2

Device Description

CLS Brevius Kinectiv Rasp Size 9

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
No
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
JDL Prosthesis, hip, semi-constrained (metal cemented acetabular component)
KWA Prosthesis, hip, semi-constrained (metal uncemented acetabular component)
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
KWL Prosthesis, hip, hemi-, femoral, metal

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 00889024280786

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 9