FDA UDI In Commercial Distribution 🇺🇸 United States

TMJ SYSTEM

DI: 00841036057442 · Model: 99-6577 · BIOMET MICROFIXATION, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TMJ SYSTEM
Primary DI
00841036057442
Version / Model
99-6577
Catalog Number
99-6577
Company Name
BIOMET MICROFIXATION, INC
Labeler DUNS
046189866
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-17
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
7fbf552c-33bd-4227-ad32-2ad788600121

Device Description

2.0X7MM FOSSA CROSS-DRIVE SCREW

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
Yes
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
JEY Plate, Bone

GMDN Terms

Code Name
46638 Craniofacial bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00841036057442
Package 00841036069421

Customer Contacts

Phone
904-741-4400

Premarket Submissions

Submission Number Supplement Number
K910038 000