FDA UDI In Commercial Distribution 🇺🇸 United States

SUPER REVO

DI: 10845854030844 · Model: C6142 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SUPER REVO
Primary DI
10845854030844
Version / Model
C6142
Catalog Number
C6142
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-06
Public Version
2
Public Version Date
2022-09-22
Public Version Status
Update
Public Device Record Key
de9c5f6b-f344-4073-8ede-9259d02ec455

Device Description

SUPER REVO REUSABLE DRIVER

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
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Primary 10845854030844
Direct Marking 20845854030841

Customer Contacts