FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00845854025461 · Model: 8720 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00845854025461
Version / Model
8720
Catalog Number
8720
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2022-09-21
Public Version Status
Update
Public Device Record Key
eda0df5d-d0fe-40ef-838e-a7123fe2feb6
Distribution End Date
2022-09-20

Device Description

9MM RECTANGULAR PATELLAR TENDOR GRAFT TEMPLATE

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
HRX ARTHROSCOPE

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Direct Marking 20845854025465
Primary 00845854025461

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Rectangular Patellar Tendon Graft Template