FDA UDI In Commercial Distribution 🇺🇸 United States

BLUEPRINT™ PATIENT SPECIFIC INSTRUMENTATION

DI: 93700386998976 · Model: MWJ004 · TORNIER
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BLUEPRINT™ PATIENT SPECIFIC INSTRUMENTATION
Primary DI
93700386998976
Version / Model
MWJ004
Catalog Number
MWJ004
Company Name
TORNIER
Labeler DUNS
260324876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-20
Public Version
5
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
c247878a-5e05-4b36-be55-4b7c0e24c71d

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
Yes
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
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 93700386998976

Customer Contacts