FDA UDI In Commercial Distribution 🇺🇸 United States

Transtrack Patient Roller 67

DI: 00842430107412 · Model: 900 · MIZUHO ORTHOPEDIC SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Transtrack Patient Roller 67
Primary DI
00842430107412
Version / Model
900
Catalog Number
900
Company Name
MIZUHO ORTHOPEDIC SYSTEMS, INC.
Labeler DUNS
084527241
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-19
Public Version
1
Public Version Date
2023-09-27
Public Version Status
New
Public Device Record Key
96071607-03b2-42da-8485-38c8643f7ed6

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
FMR Device, Transfer, Patient, Manual

GMDN Terms

Code Name
37163 Patient transfer sliding mat

Identifiers

Type ID
Primary 00842430107412

Customer Contacts