EndoVue

GUDID 00818089022383

ENDOVUE, 32", AMERICAS, JAPAN, BC-WU32-N1418

Nds Surgical Imaging LLC

Image display monitor, colour
Primary Device ID00818089022383
NIH Device Record Key5d72b22a-8add-4a10-99d0-ab0735655f30
Commercial Distribution Discontinuation2022-06-27
Commercial Distribution StatusNot in Commercial Distribution
Brand NameEndoVue
Version Model Number90K0081
Company DUNS081712583
Company NameNds Surgical Imaging LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100818089022383 [Primary]

FDA Product Code

KQMCamera, Surgical And Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-07-04
Device Publish Date2022-06-24

On-Brand Devices [EndoVue]

00818089022956ENDOVUE, 24", AMERICAS, JAPAN, EMEA, BC-WU24-N1418
00818089022949ENDOVUE, 21", AMERICAS, JAPAN, EMEA, BC-WU21-N1418
00818089022420ENDOVUE, 24", EMERGING MARKET, BC-WU24-N1418
00818089022413ENDOVUE, 21", EMERGING MARKET, BC-WU21-N1418
00818089021942ENDOVUE, 21", EUROPE, BC-WU21-N1418
00818089021935ENDOVUE, 21", CHINA, BC-WU21-N1418
00818089021928ENDOVUE, 19", EUROPE, BC-SX19-N1418
00818089021911ENDOVUE, 19", CHINA, BC-SX19-N1418
00818089021904ENDOVUE, 19", AMERICAS, JAPAN, BC-SX19-N1418
00818089020044ENDOVUE PLUS, 19" LED, BC-SX19-A1417
00818089020037ENDOVUE PLUS, 15" LED, BC-X15-A1417
00818089020020ENDOVUE PLUS, 24", BC-WU24-A1417
00818089022369ENDOVUE, 21", AMERICAS, JAPAN, BC-WU21-N1418
00851455007997ENDOVUE PLUS 4K 55", 12G-SDI, Quad-Link SDI
00851455007980EndoVue Plus 4K 55”
00851455007973ENDOVUE PLUS 4K 32", Quad-Link SDI, BC-WK32-A1B20
00851455007966ENDOVUE PLUS 4K 32", BC-WK32-A1B00
00818089022963EndoVue Plus 4K, America, Japan, EMEA, BC-WK32-A1B00
00818089022383ENDOVUE, 32", AMERICAS, JAPAN, BC-WU32-N1418
00818089022376ENDOVUE, 24", AMERICAS, JAPAN, BC-WU24-N1418
00818089022000ENDOVUE PLUS 24" EU (2018 Series) BC-WU24-A1417
00818089021997ENDOVUE PLUS 24" CHINA (2018 Series) BC-WU24-A1417
00818089021980ENDOVUE PLUS 24" (2018 Series) BC-WU24-A1417
00818089021973ENDOVUE, 32", EUROPE, BC-WU32-N1418
00818089021966ENDOVUE, 32", CHINA, BC-WU32-N1418
00818089021959ENDOVUE, 24", CHINA, BC-WU24-N1418
00818089022970EndoVue Plus 4K 32”, Quad-link SDI, America, Japan, EMEA, BC-WK32-A1B20
00818089022604ENDOVUE PLUS 4K 32", QUAD-LINK SDI, EMEA, BC-WK32-A1B20
00818089022598ENDOVUE PLUS 4K 32", EMEA, BC-WK32-A1B00
00818089022581ENDOVUE PLUS 4K 32", QUAD-LINK SDI, CHINA, BC-WK32-A1B20
00818089022574ENDOVUE PLUS 4K 32", CHINA, BC-WK32-A1B00
00818089022987SMITH & NEPHEW, ENDOVUE PLUS 4K 32", TOUCH, BC-WK32-C1B00
00818089021300ENDOVUE 15" LED, CUSTOM KARL STORZ US, BC-X15-A1417
00818089021294ENDOVUE 15" LED, CUSTOM KARL STORZ GMBH, BC-X15-A1417
00818089021010CUSTOM MED15, 24" ENDOVUE, BC-WU24-A1417
00851455007805ENDOVUE, 32", CUSTOM DEPUY SYNTHES, BRAZIL, BC-WU32-N1418
00851455007737ENDOVUE, 32", CUSTOM DEPUY SYNTHES, CHINA, BC-WU32-N1418
00818089022505KARL STORZ CHINA, ENDOVUE, 24", CHINA, BC-WU24-N1418
00818089021287PENTAX EMEA, ENDOVUE, 32", EMEA, BC-WU32-N1418
00818089021263PENTAX EMEA, ENDOVUE, 21", EMEA, BC-WU21-N1418
00818089021232PENTAX, ENDOVUE, 32", AMERICAS, BC-WU32-N1418
00818089023021ZIMMER BIOMET, ENDOVUE PLUS 4K 32", BC-WK32-A1B00 (Zimmer Biomet Distributed, Ref # 84-24-3100)
00818089021270PENTAX EMEA, ENDOVUE, 24", EMEA, US, BC-WU24-N1418

Trademark Results [EndoVue]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ENDOVUE
ENDOVUE
77765516 3742246 Live/Registered
NOVANTA INC.
2009-06-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.