FDA UDI In Commercial Distribution 🇺🇸 United States

GENESYS CROSSFT

DI: 10845854028223 · Model: PFT-55MB · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GENESYS CROSSFT
Primary DI
10845854028223
Version / Model
PFT-55MB
Catalog Number
PFT-55MB
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-30
Public Version
4
Public Version Date
2023-01-12
Public Version Status
Update
Public Device Record Key
e3dd8958-ce3e-4a04-860e-b46689beba7e

Device Description

GENESYS CROSSFT PUNCH, 5.5MM

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
36167 Orthopaedic broach

Identifiers

Type ID
Primary 10845854028223
Direct Marking 20845854028220

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 5.5MM

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY