FDA UDI In Commercial Distribution 🇺🇸 United States

Pedi Board

DI: 00766923025215 · Model: 02521 · PEDICRAFT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pedi Board
Primary DI
00766923025215
Version / Model
02521
Catalog Number
02521
Company Name
PEDICRAFT, INC.
Labeler DUNS
041136011
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-07
Public Version
1
Public Version Date
2023-06-15
Public Version Status
New
Public Device Record Key
ba312c3b-5f66-43bc-9bb9-596a65a5d032

Device Description

Pedi Board 1x3

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NOD Board, Arm (With Cover), Non-Sterile

GMDN Terms

Code Name
37047 Arm procedure positioner, reusable

Identifiers

Type ID
Package 10766923025212
Primary 00766923025215

Customer Contacts

Phone
904-396-9627