FDA UDI In Commercial Distribution 🇺🇸 United States

MatrixMANDIBLE

DI: 10887587012292 · Model: 03.503.166 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MatrixMANDIBLE
Primary DI
10887587012292
Version / Model
03.503.166
Catalog Number
03503166
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
5
Public Version Date
2022-04-25
Public Version Status
Update
Public Device Record Key
fac91776-d6ec-4be0-ab5a-6f5d00d67f51

Device Description

MATRIXMANDIBLE BENDNG TEMPLATE F/1.25MM THICK ANGLE PLATES

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
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
HWT TEMPLATE

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Secondary H980035031660
Primary 10887587012292

Customer Contacts