FDA UDI Not in Commercial Distribution 🇺🇸 United States

PINN-ACL

DI: 10845854034668 · Model: CPS-8902 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PINN-ACL
Primary DI
10845854034668
Version / Model
CPS-8902
Catalog Number
CPS-8902
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
2
Public Version Date
2022-06-09
Public Version Status
Update
Public Device Record Key
7cc5230a-bac0-4453-b8a5-0a61fb575fa7
Distribution End Date
2022-06-08

Device Description

PINN-ACL CROSSPIN U-GUIDE

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
Yes
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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
47831 Orthopaedic implantation sleeve, reusable

Identifiers

Type ID
Direct Marking 20845854034665
Primary 10845854034668

Customer Contacts