FDA UDI In Commercial Distribution 🇺🇸 United States

Fibernex

DI: B050LF0101X9400 · Model: LF0101X940 · TYPENEX MEDICAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Fibernex
Primary DI
B050LF0101X9400
Version / Model
LF0101X940
Company Name
TYPENEX MEDICAL LLC
Labeler DUNS
600850213
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-27
Public Version
4
Public Version Date
2023-12-13
Public Version Status
Update
Public Device Record Key
3ebc2f41-9752-4ee8-a061-2c05bff72b9f

Device Description

Fibernex 940 micrometer Single Use Holmium Laser Fiber

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
Labeling does not contain MRI Safety Information
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
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
36037 Laser lithotripsy system

Identifiers

Type ID
Package B050LF0101X9403
Primary B050LF0101X9400

Customer Contacts

Phone
312-888-4064

Device Sizes

Type Value Unit Text
Outer Diameter 940 Micrometer