FDA UDI Not in Commercial Distribution 🇺🇸 United States

iDuo® Tibial Kit

DI: M572RBK1011113011 · Model: RBK101111301 · Conformis, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iDuo® Tibial Kit
Primary DI
M572RBK1011113011
Version / Model
RBK101111301
Catalog Number
RBK1011113
Company Name
Conformis, Inc.
Labeler DUNS
808821883
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-26
Public Version
3
Public Version Date
2022-08-16
Public Version Status
Update
Public Device Record Key
ca3a107e-09ff-4f98-b988-17ef439fc06c
Distribution End Date
2022-08-15

Device Description

N/A

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NPJ Prosthesis, Knee Patellofemorotibial, Partial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
OOG Knee Arthroplasty Implantation System

GMDN Terms

Code Name
58228 Bicompartmental knee prosthesis

Identifiers

Type ID
Primary M572RBK1011113011

Customer Contacts

Phone
781-345-9001

Device Sizes

Type Value Unit Text
Device Size Text, specify Patient Specific