FDA UDI In Commercial Distribution 🇺🇸 United States

FOLIFLEX PRO

DI: E23912401250501 · Model: 1240125050 · Dreve Dentamid GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FOLIFLEX PRO
Primary DI
E23912401250501
Version / Model
1240125050
Catalog Number
1240125050
Company Name
Dreve Dentamid GmbH
Labeler DUNS
388000846
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-31
Public Version
1
Public Version Date
2024-11-08
Public Version Status
New
Public Device Record Key
4fd25e86-5844-413c-9b41-cf0aded66cf6

Device Description

No.

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KMY POSITIONER, TOOTH, PREFORMED

GMDN Terms

Code Name
58288 Dental appliance fabrication material, thermoplastic

Identifiers

Type ID
Primary E23912401250501

Customer Contacts

Phone
+49230388070

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Storage Environment Temperature
Temperature Range
18 – 28 Degrees Celsius