Primary Device ID | 05060940370163 |
NIH Device Record Key | e0fc0e86-a134-4c2f-8f15-db0faecd6d75 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VaryFlex Reciprocating, VFRF Medium, 25mm |
Version Model Number | VFRF2525 |
Company DUNS | 224419290 |
Company Name | ENDOPERFECTION LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060940370163 [Primary] |
EKS | File, Pulp Canal, Endodontic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-05 |
Device Publish Date | 2024-01-28 |
05060940379418 - VaryFlex OR, VFOR, 20/07, 19mm | 2025-04-10 |
05060940376905 - VaryFlex Neo, 30/04, 25mm | 2024-04-12 |
05060940376912 - VaryFlex Neo, 35/04, 25mm | 2024-04-12 |
05060940376929 - VaryFlex Neo, 40/04, 25mm | 2024-04-12 |
05060940376936 - VaryFlex Neo, 50/04, 25mm | 2024-04-12 |
05060940376943 - VaryFlex Neo, 15/04, 31mm | 2024-04-12 |
05060940376950 - VaryFlex Neo, 25/04, 31mm | 2024-04-12 |
05060940376967 - VaryFlex Neo, 30/04, 31mm | 2024-04-12 |