FDA UDI In Commercial Distribution 🇺🇸 United States

REVO

DI: 20845854019785 · Model: C6101H · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REVO
Primary DI
20845854019785
Version / Model
C6101H
Catalog Number
C6101H
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
6
Public Version Date
2024-01-11
Public Version Status
Update
Public Device Record Key
a438b0e5-5005-4e6b-854a-808593a6bfe5

Device Description

4MM REVO ANCHOR, PRETHREADED, No. 2 (5 METRIC) HI-FI

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBI FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE

GMDN Terms

Code Name
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Primary 20845854019785

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K963932 000

Device Sizes

Type Value Unit Text
Outer Diameter 4 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY