FDA UDI In Commercial Distribution 🇺🇸 United States

BioPrep

DI: 04546540039637 · Model: 0206710000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BioPrep
Primary DI
04546540039637
Version / Model
0206710000
Catalog Number
0206-710-000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-23
Public Version
4
Public Version Date
2020-11-05
Public Version Status
Update
Public Device Record Key
b902d0af-b218-4a97-9454-beffacffb400

Device Description

Bone Preparation Kit

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JDK Prosthesis, hip, cement restrictor

GMDN Terms

Code Name
35217 Orthopaedic cement, non-antimicrobial

Identifiers

Type ID
Package 34546540039638
Primary 04546540039637

Customer Contacts