FDA UDI In Commercial Distribution 🇺🇸 United States

FENTEX

DI: 04250407709778 · Model: 109113FX · FENTEX medical GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FENTEX
Primary DI
04250407709778
Version / Model
109113FX
Catalog Number
109113FX
Company Name
FENTEX medical GmbH
Labeler DUNS
507221724
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-07
Public Version
1
Public Version Date
2022-12-15
Public Version Status
New
Public Device Record Key
ffca9531-2b7c-4d59-bb80-38e8c48b85b9

Device Description

Dressing Forceps Standard, straight 13 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
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 04250407709778

Customer Contacts