FDA UDI In Commercial Distribution 🇺🇸 United States

ParaPost FiberLux

DI: D661SBPF17151 · Model: SBPF1715 · COLTENE/WHALEDENT INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
ParaPost FiberLux
Primary DI
D661SBPF17151
Version / Model
SBPF1715
Company Name
COLTENE/WHALEDENT INC
Labeler DUNS
622185718
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2021-01-04
Public Version
1
Public Version Date
2021-01-12
Public Version Status
New
Public Device Record Key
988e3682-a502-4ce9-8ec6-7eddcafee507

Device Description

STERILE PARAPOST FIBERLUX SIZE 5

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ELR Post, Root Canal

GMDN Terms

Code Name
38609 Root canal post, preformed

Identifiers

Type ID
Unit of Use D661SBPF17150
Primary D661SBPF17151