FDA UDI In Commercial Distribution 🇺🇸 United States

REPIPHYSIS®

DI: M684255120131 · Model: 25512013 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REPIPHYSIS®
Primary DI
M684255120131
Version / Model
25512013
Catalog Number
25512013
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-29
Public Version
1
Public Version Date
2018-10-01
Public Version Status
New
Public Device Record Key
d2bf593b-1d49-4d4a-9524-e0a7a10ef8dd

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HXW BENDER

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary M684255120131

Customer Contacts