FDA UDI In Commercial Distribution 🇺🇸 United States

SLR BIPOLAR

DI: M684170032041 · Model: 17003204 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SLR BIPOLAR
Primary DI
M684170032041
Version / Model
17003204
Catalog Number
17003204
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-20
Public Version
3
Public Version Date
2020-09-09
Public Version Status
Update
Public Device Record Key
752c8d0c-985e-41da-95db-0b8a0ef48b17

Device Description

SLR BIPOLAR INSERT 48-50mm X 32mm ID

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

GMDN Terms

Code Name
33695 Bipolar femoral head outer component, hemiarthroplasty

Identifiers

Type ID
Direct Marking 17003204
Primary M684170032041

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 32 Millimeter