FDA UDI In Commercial Distribution 🇺🇸 United States

Pedimax II - Pedicular Screw Spinal System

DI: 07899258600222 · Model: Monoaxial Pedicle Screw · GM DOS REIS INDUSTRIA E COMERCIO LTDA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pedimax II - Pedicular Screw Spinal System
Primary DI
07899258600222
Version / Model
Monoaxial Pedicle Screw
Catalog Number
176-11-30
Company Name
GM DOS REIS INDUSTRIA E COMERCIO LTDA
Labeler DUNS
900865213
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-18
Public Version
1
Public Version Date
2024-01-26
Public Version Status
New
Public Device Record Key
649a9d18-a309-4fb7-bbf8-2e02b4ec5134

Device Description

PEDIMAX II MONOAXIAL PEDICLE SCREWØ6.2x30.0mm

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
MR Conditional
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
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 07899258600222

Premarket Submissions

Submission Number Supplement Number
K180626 000