FDA UDI In Commercial Distribution 🇺🇸 United States

GENESYS CROSSFT

DI: 20845854042677 · Model: CFBC-4502NB · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GENESYS CROSSFT
Primary DI
20845854042677
Version / Model
CFBC-4502NB
Catalog Number
CFBC-4502NB
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
5
Public Version Date
2019-03-21
Public Version Status
Update
Public Device Record Key
6e182dd2-429b-4e98-99cd-7dd8435e086c

Device Description

GENESYS CROSSFT 4.5MM SUTURE ANCHOR, W/ 2 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES

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 Safe
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
MAI FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE

GMDN Terms

Code Name
45061 Tendon/ligament bone anchor, bioabsorbable

Identifiers

Type ID
Primary 20845854042677

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K101100 000

Device Sizes

Type Value Unit Text
Outer Diameter 4.5 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
– 104 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY