FDA UDI In Commercial Distribution 🇺🇸 United States

LINERS, BOOT, ORTHO, 1/PR

DI: 00842430112676 · Model: 229 · MIZUHO ORTHOPEDIC SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
LINERS, BOOT, ORTHO, 1/PR
Primary DI
00842430112676
Version / Model
229
Catalog Number
229
Company Name
MIZUHO ORTHOPEDIC SYSTEMS, INC.
Labeler DUNS
084527241
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2020-09-30
Public Version
2
Public Version Date
2020-11-06
Public Version Status
Update
Public Device Record Key
74df1ed3-975d-4e08-8406-66b3737ffb6d

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FMP Protector, Skin Pressure

GMDN Terms

Code Name
36295 Foot friction/impact protector

Identifiers

Type ID
Unit of Use 00842430114328
Primary 00842430112676

Customer Contacts