FDA UDI In Commercial Distribution 🇺🇸 United States

FENTEX

DI: 04250407767853 · Model: 532138FXF · FENTEX medical GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FENTEX
Primary DI
04250407767853
Version / Model
532138FXF
Catalog Number
532138FXF
Company Name
FENTEX medical GmbH
Labeler DUNS
507221724
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-12
Public Version
1
Public Version Date
2022-12-20
Public Version Status
New
Public Device Record Key
b1eec482-ff0f-4af9-97ed-393be3431eb0

Device Description

Atraumatic Vocal Cord Retractor self-retaining, with flush connector WL 24 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
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 04250407767853

Customer Contacts