FDA UDI In Commercial Distribution 🇺🇸 United States

CLS® Brevius® Kinectiv®

DI: 00889024280830 · Model: 01.00297.150 · Zimmer GmbH
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CLS® Brevius® Kinectiv®
Primary DI
00889024280830
Version / Model
01.00297.150
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
ab76ba55-77f7-4eab-9c1b-3c0f9b7b7911

Device Description

CLS Brevius Kinectiv Rasp Size 15

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
KWA Prosthesis, hip, semi-constrained (metal uncemented acetabular component)
JDL Prosthesis, hip, semi-constrained (metal cemented acetabular component)
KWL Prosthesis, hip, hemi-, femoral, metal
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 00889024280830

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 15