FDA UDI In Commercial Distribution 🇺🇸 United States

PKIT, ULTRA SHOULDER, REHAB SLING

DI: 00842430109089 · Model: 5348-1 · MIZUHO ORTHOPEDIC SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
PKIT, ULTRA SHOULDER, REHAB SLING
Primary DI
00842430109089
Version / Model
5348-1
Catalog Number
5348
Company Name
MIZUHO ORTHOPEDIC SYSTEMS, INC.
Labeler DUNS
084527241
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-17
Public Version
6
Public Version Date
2023-09-19
Public Version Status
Update
Public Device Record Key
d6b1aab3-7dd1-49e8-969a-33c3c552faf0

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
FMQ Restraint, Protective

GMDN Terms

Code Name
62619 Surgical linen/cushion set

Identifiers

Type ID
Package 10842430109086
Primary 00842430109089
Package 20842430109083

Customer Contacts