FDA UDI In Commercial Distribution 🇺🇸 United States

OrthoPediatrics Hardware Removal

DI: 00840194465236 · Model: 01-9200-0135 · ORTHOPEDIATRICS CORP.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
OrthoPediatrics Hardware Removal
Primary DI
00840194465236
Version / Model
01-9200-0135
Catalog Number
01-9200-0135
Company Name
ORTHOPEDIATRICS CORP.
Labeler DUNS
796416191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-15
Public Version
1
Public Version Date
2024-04-23
Public Version Status
New
Public Device Record Key
a7cce1f3-21a8-4807-9939-032a6e594369

Device Description

Driver, Cannulated 3.5mm Hex

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
HXX SCREWDRIVER
KIJ Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary 00840194465236