FDA UDI In Commercial Distribution 🇺🇸 United States

PediNail

DI: 00840194444859 · Model: 11-1500-002-S · ORTHOPEDIATRICS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PediNail
Primary DI
00840194444859
Version / Model
11-1500-002-S
Catalog Number
11-1500-002-S
Company Name
ORTHOPEDIATRICS CORP.
Labeler DUNS
796416191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-05
Public Version
1
Public Version Date
2025-06-13
Public Version Status
New
Public Device Record Key
b886e4ad-450d-454d-9160-94187d676d11

Device Description

2.0MM SMOOTH GUIDE WIRE

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FZX Guide, surgical, instrument

GMDN Terms

Code Name
62729 Orthopaedic guidewire, single-use

Identifiers

Type ID
Primary 00840194444859

Customer Contacts