FDA UDI In Commercial Distribution 🇺🇸 United States

NEOFIX

DI: 07899893206223 · Model: 903.522 · Neoortho Produtos Ortopédicos S/A.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NEOFIX
Primary DI
07899893206223
Version / Model
903.522
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
2015-10-21
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
e11c498c-3fcc-49b4-9329-c960eb66eae7

Device Description

Emergency Standard Cortical Screw D2.3x9.0mm

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
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 07899893206223

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K142419 000