FDA UDI In Commercial Distribution 🇺🇸 United States

FENTEX

DI: 04250407722067 · Model: 221200FX · FENTEX medical GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FENTEX
Primary DI
04250407722067
Version / Model
221200FX
Catalog Number
221200FX
Company Name
FENTEX medical GmbH
Labeler DUNS
507221724
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-09
Public Version
1
Public Version Date
2022-12-19
Public Version Status
New
Public Device Record Key
28a8b0ac-b1a4-4ac3-ae4a-49f824e7dfe3

Device Description

Septum Gouge by Killian-Claus bayonet-shaped, V-shaped blade 16.5 cm, width 5 mm

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
No
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
LRC INSTRUMENT, ENT MANUAL SURGICAL

GMDN Terms

Code Name
35914 Nasal gouge

Identifiers

Type ID
Primary 04250407722067

Customer Contacts