FDA UDI In Commercial Distribution 🇺🇸 United States

BeautiBond/Beautifil

DI: E2352000BF030 · Model: 001 · SHOFU DENTAL CORPORATION
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BeautiBond/Beautifil
Primary DI
E2352000BF030
Version / Model
001
Catalog Number
2000FF03
Company Name
SHOFU DENTAL CORPORATION
Labeler DUNS
054618202
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-09
Public Version
1
Public Version Date
2018-09-10
Public Version Status
New
Public Device Record Key
bd66fd0f-975c-4d0d-a4b2-e1cd967aed1b

Device Description

Beautifil Flow Plus/Beautibond Low Flow Kit. Contains DI's: E23520140, E23520150, E23520160, E23520180, E23517820

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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

GMDN Terms

Code Name
35870 Dental composite resin

Identifiers

Type ID
Primary E2352000BF030

Customer Contacts

Phone
760-566-3528

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
1 – 30 Degrees Celsius