FDA UDI Not in Commercial Distribution 🇺🇸 United States

BIOLIGHT

DI: 66714700001293 · Model: BDT13 · Synca Marketing Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
BIOLIGHT
Primary DI
66714700001293
Version / Model
BDT13
Company Name
Synca Marketing Inc
Labeler DUNS
247111768
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-27
Public Version
3
Public Version Date
2021-07-27
Public Version Status
Update
Public Device Record Key
97b6ddb5-2b58-4bab-871c-596083625d26
Distribution End Date
2021-07-26

Device Description

BIOLIGHT DUAL REFILL #3

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No

Product Codes

Code Name
ELR Post, Root Canal

GMDN Terms

Code Name
38609 Root canal post, preformed

Identifiers

Type ID
Primary 66714700001293
Unit of Use 00667147001293

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 3