FDA UDI In Commercial Distribution 🇺🇸 United States

MatrixMIDFACE

DI: 20887587018741 · Model: 04.503.203.20 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
20

Basic Information

Brand Name
MatrixMIDFACE
Primary DI
20887587018741
Version / Model
04.503.203.20
Catalog Number
0450320320
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
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
78fbfa97-a5dc-4f6a-a636-4d7bfd63e9b2

Device Description

TI MATRIXMIDFACE SCREW SELF-TAPPING 3MM

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
Primary 20887587018741
Unit of Use 80887587018743
Secondary H98004503203200

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K050608 000