FDA UDI In Commercial Distribution 🇺🇸 United States

PediPlates

DI: 00841132145166 · Model: 01-1012-0012 · ORTHOPEDIATRICS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PediPlates
Primary DI
00841132145166
Version / Model
01-1012-0012
Catalog Number
01-1012-0012
Company Name
ORTHOPEDIATRICS CORP.
Labeler DUNS
796416191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-21
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
3850a7d6-b0b9-4ea5-8139-698abc1aeda1

Device Description

Ti PediPlates Cannulated Screw Caddy Lid, LP

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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
44896 Growth-correction orthopaedic fixation plate kit

Identifiers

Type ID
Primary 00841132145166

Customer Contacts