FDA UDI Not in Commercial Distribution 🇺🇸 United States

FENTEX

DI: 04250407720872 · Model: 187915FX · FENTEX medical GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FENTEX
Primary DI
04250407720872
Version / Model
187915FX
Catalog Number
187915FX
Company Name
FENTEX medical GmbH
Labeler DUNS
507221724
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
4
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
54c24a69-88a8-45a4-8f7a-f101810917f5
Distribution End Date
2022-12-31

Device Description

Silicone Mat blue stems Dimensions: 500 x 320 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
MMO TRAY, SURGICAL, ENT

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 04250407720872

Customer Contacts