FDA UDI In Commercial Distribution 🇺🇸 United States

Shoulder iD

DI: 03700434023718 · Model: MWJ007 · TORNIER
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Shoulder iD
Primary DI
03700434023718
Version / Model
MWJ007
Catalog Number
MWJ007
Company Name
TORNIER
Labeler DUNS
260324876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-23
Public Version
1
Public Version Date
2024-05-31
Public Version Status
New
Public Device Record Key
08816b31-987e-48f1-9722-21fabf579e07

Device Description

BLUEPRINT Primary Reversed Glenoid Guide

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
QHE Shoulder arthroplasty implantation system

GMDN Terms

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

Identifiers

Type ID
Primary 03700434023718

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 25 Millimeter