FDA UDI In Commercial Distribution 🇺🇸 United States

MEDI

DI: 00636257045404 · Model: RKIT9002 · MEDI MANUFACTURING, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MEDI
Primary DI
00636257045404
Version / Model
RKIT9002
Company Name
MEDI MANUFACTURING, INC.
Labeler DUNS
960754430
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-25
Public Version
1
Public Version Date
2023-08-02
Public Version Status
New
Public Device Record Key
5d7c054b-93d6-4279-ba61-55665c7f4823

Device Description

PROTECT.4 EVO PAD STRAP KIT, LEFT, SM

Device Characteristics

Single Use
Yes
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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ITQ JOINT, KNEE, EXTERNAL BRACE

GMDN Terms

Code Name
41065 Knee support orthosis

Identifiers

Type ID
Primary 00636257045404

Customer Contacts