FDA UDI In Commercial Distribution 🇺🇸 United States

FENTEX

DI: 04250407702137 · Model: 023803FX · FENTEX medical GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FENTEX
Primary DI
04250407702137
Version / Model
023803FX
Catalog Number
023803FX
Company Name
FENTEX medical GmbH
Labeler DUNS
507221724
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-05
Public Version
1
Public Version Date
2022-12-13
Public Version Status
New
Public Device Record Key
938afff7-fca6-4b99-90d7-070e6db8dbd3

Device Description

Ear Hook with ball end, 45° 15.5 cm

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
33433 ENT probe, reusable

Identifiers

Type ID
Primary 04250407702137

Customer Contacts