FDA UDI In Commercial Distribution 🇺🇸 United States

NEOFIX

DI: 07899893204311 · Model: 900.959 · Neoortho Produtos Ortopédicos S/A.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NEOFIX
Primary DI
07899893204311
Version / Model
900.959
Company Name
Neoortho Produtos Ortopédicos S/A.
Labeler DUNS
914644351
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-19
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
db88c4b1-cddd-41a9-b26c-cb6e0ad2d5f7

Device Description

Right 2.0 Condylar Plate

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
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
HRS Plate, Fixation, Bone

GMDN Terms

Code Name
61573 Orthopaedic fixation plate, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 07899893204311

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K142419 000