FDA UDI In Commercial Distribution 🇺🇸 United States

PediFlex

DI: 00840194493727 · Model: 01-1001-0002 · ORTHOPEDIATRICS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PediFlex
Primary DI
00840194493727
Version / Model
01-1001-0002
Catalog Number
01-1001-0002
Company Name
ORTHOPEDIATRICS CORP.
Labeler DUNS
796416191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-21
Public Version
1
Public Version Date
2025-03-31
Public Version Status
New
Public Device Record Key
f221df2e-05bc-43ab-a76b-c6ea9a42096c

Device Description

Curved Awl

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
HWJ AWL

GMDN Terms

Code Name
15275 Bone awl, reusable

Identifiers

Type ID
Primary 00840194493727

Customer Contacts