FDA UDI Not in Commercial Distribution 🇺🇸 United States

Matrix

DI: 10705034719306 · Model: 03.632.089 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Matrix
Primary DI
10705034719306
Version / Model
03.632.089
Catalog Number
03632089
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
5
Public Version Date
2020-09-17
Public Version Status
Update
Public Device Record Key
f50f68a3-3c43-4d12-b5b4-2f6d4f71494c
Distribution End Date
2020-09-17

Device Description

FOOTED DISTRACTOR TIP FOR MATRIX DISTRACTOR

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
No
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44378 Bone distraction forceps

Identifiers

Type ID
Direct Marking 07611819388062
Secondary H981036320890
Primary 10705034719306

Customer Contacts