Primary Device ID | 00677964082986 |
NIH Device Record Key | 2f642226-ef18-4a43-aacb-1feabc256010 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SCOPE BUDDY PLUS TUBING |
Version Model Number | SB-110-HU1012 |
Company DUNS | 068199363 |
Company Name | MEDIVATORS INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00677964082986 [Primary] |
GS1 | 10677964082983 [Package] Package: Box [30 Units] In Commercial Distribution |
GS1 | 20677964082980 [Package] Contains: 10677964082983 Package: Case [30 Units] In Commercial Distribution |
FEB | Accessories, Cleaning, For Endoscope |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2019-06-04 |
00677964092046 | SB-110-HU1016 |
00677964082993 | SB-110-HU1015 |
00677964082986 | SB-110-HU1012 |
00677964082979 | SB-110-HU1011 |
00677964082962 | SB-110-HU1008 |
00677964082955 | SB-110-HU1010 |
00677964082948 | SB-110-HU1009 |
00677964082924 | SB-110-HU1007 |
40677964021983 | 24 Hour Tubing for FUJIFILM 700 Endoscopes |