FDA UDI In Commercial Distribution 🇺🇸 United States

REVO

DI: 10845854030837 · Model: C6128 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
REVO
Primary DI
10845854030837
Version / Model
C6128
Catalog Number
C6128
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
3
Public Version Date
2023-05-25
Public Version Status
Update
Public Device Record Key
4c30ca5c-41b5-46eb-bea7-d71c1ee5cfaa

Device Description

MINI-REVO TAP

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
HWX TAP, BONE

GMDN Terms

Code Name
17507 Bone tap, reusable

Identifiers

Type ID
Direct Marking 20845854030834
Primary 10845854030837

Customer Contacts