FDA UDI In Commercial Distribution 🇺🇸 United States

MatrixMIDFACE

DI: 10887587019178 · Model: 04.503.226.01 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MatrixMIDFACE
Primary DI
10887587019178
Version / Model
04.503.226.01
Catalog Number
0450322601
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
6
Public Version Date
2024-02-27
Public Version Status
Update
Public Device Record Key
61790270-8b7c-471b-a921-05b62cc1bf00

Device Description

TI MATRIXMIDFACE SCREW SELF-DRILLING 6MM

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
DZL SCREW, FIXATION, INTRAOSSEOUS
JEY PLATE, BONE

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Secondary H98004503226010
Primary 10887587019178

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K050608 000
K083388 000