Primary Device ID | 00857834006339 |
NIH Device Record Key | e945bd68-7775-4318-bfff-939e1c97ff47 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ERCP |
Version Model Number | GI127 |
Company DUNS | 080645456 |
Company Name | HERAEUS MEDICAL COMPONENTS, LLC |
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 | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | true |
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 | 00857834006339 [Primary] |
OCY | Endoscopic Guidewire, Gastroenterology-Urology |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-10-05 |
Device Publish Date | 2016-09-21 |
00857834006384 | GI132 |
00857834006377 | GI131 |
00857834006360 | GI130 |
00857834006353 | GI129 |
00857834006346 | GI128 |
00857834006339 | GI127 |
00857834006322 | GI126 |
00857834006315 | GI125 |
00857834006308 | GI124 |
00857834006292 | GI123 |
00857834006285 | GI122 |
00857834006278 | GI121 |
00857834006261 | GI120 |
00857834006254 | GI119 |
00857834006247 | GI118 |
00857834006230 | GI117 |
00857834006223 | GI116 |
00857834006216 | GI115 |
00857834006209 | GI114 |
00857834006193 | GI113 |
00857834006186 | GI112 |
00857834006179 | GI111 |
00857834006162 | GI110 |
00857834006155 | GI109 |
00857834006148 | GI108 |
00857834006131 | GI107 |
00857834006124 | GI106 |
00857834006117 | GI105 |
00857834006100 | GI104 |
00857834006094 | GI103 |
00857834006087 | GI102 |
00857834006070 | GI101 |