FDA UDI In Commercial Distribution 🇺🇸 United States

iTotal CR

DI: M572RCR0201600031 · Model: RCR-020-160003 · Conformis, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iTotal CR
Primary DI
M572RCR0201600031
Version / Model
RCR-020-160003
Catalog Number
RCR-020-1600
Company Name
Conformis, Inc.
Labeler DUNS
808821883
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-17
Public Version
1
Public Version Date
2022-08-25
Public Version Status
New
Public Device Record Key
32b10319-16f5-47a9-929b-8a84d5b8e124

Device Description

ITOTAL CR–IPOLY XE–16MM MEDIAL INSERT KIT–LEFT or right

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
MR Conditional
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
OOG Knee Arthroplasty Implantation System

GMDN Terms

Code Name
46585 Tibial insert

Identifiers

Type ID
Primary M572RCR0201600031

Customer Contacts

Phone
781-345-9001

Device Sizes

Type Value Unit Text
Device Size Text, specify Thickness 16mm