FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10197344023912 · Model: MJPR0000 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MEDLINE
Primary DI
10197344023912
Version / Model
MJPR0000
Catalog Number
MJPR0000
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-22
Public Version
1
Public Version Date
2024-07-30
Public Version Status
New
Public Device Record Key
eec1b4f2-0d86-481f-9749-9f9860770e48

Device Description

FOOT JOINT PREP KIT, STERILE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
KDD Kit, surgical instrument, disposable

GMDN Terms

Code Name
44052 Orthopaedic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 10197344023912

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Protect from freezing. Avoid excessive heat.