FDA UDI In Commercial Distribution 🇺🇸 United States

FENTEX

DI: 04250407723002 · Model: 230500FX · FENTEX medical GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FENTEX
Primary DI
04250407723002
Version / Model
230500FX
Catalog Number
230500FX
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
82ea801e-67b3-4375-9969-4254c8a1142b

Device Description

Polyp Grasping Forceps by Wigand 60° upturned WL 11 cm, spoon 6 x 14 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
62467 Surgical soft-tissue manipulation forceps, alligator, reusable

Identifiers

Type ID
Primary 04250407723002

Customer Contacts