FDA UDI In Commercial Distribution 🇺🇸 United States

MICROPORT

DI: M684201620141 · Model: 20162014 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MICROPORT
Primary DI
M684201620141
Version / Model
20162014
Catalog Number
20162014
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
1
Public Version Date
2018-10-15
Public Version Status
New
Public Device Record Key
ab4739f2-0049-43f5-ab0b-d9427e922b3a

Device Characteristics

Single Use
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary M684201620141

Customer Contacts