FDA UDI In Commercial Distribution 🇺🇸 United States

BIOLIGHT

DI: 00667147000333 · Model: BDT40 · Synca Marketing Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIOLIGHT
Primary DI
00667147000333
Version / Model
BDT40
Company Name
Synca Marketing Inc
Labeler DUNS
247111768
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-15
Public Version
1
Public Version Date
2021-07-23
Public Version Status
New
Public Device Record Key
58b61001-66ad-4d34-bcc8-08a3f5fa5019

Device Description

BIOLIGHT DUAL ADVANCED FIBER POSTS INTRO KIT

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ELR Post, Root Canal

GMDN Terms

Code Name
38609 Root canal post, preformed

Identifiers

Type ID
Primary 00667147000333

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Biolight dual post # 0.5 - 1 - 2 - 3 Biolight reamer # 0.5 - 1 - 2 -3