FDA UDI In Commercial Distribution 🇺🇸 United States

Biodentine XP 500

DI: 03701398102143 · Model: 01C0720 · SEPTODONT SAS SPECIALITES SEPTODONT
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Biodentine XP 500
Primary DI
03701398102143
Version / Model
01C0720
Catalog Number
01C0720
Company Name
SEPTODONT SAS SPECIALITES SEPTODONT
Labeler DUNS
275273795
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-02-07
Public Version
1
Public Version Date
2022-02-15
Public Version Status
New
Public Device Record Key
56dd7b96-a589-40dc-98b0-391c023219c1

Device Description

Bioactive dentin substitute

Device Characteristics

Single Use
Yes
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
No
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
KIF Resin, Root Canal Filling

GMDN Terms

Code Name
60510 Hygroscopic dental cement

Identifiers

Type ID
Unit of Use 03701398101993
Primary 03701398102143

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
41 – 77 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Protect from Moisture