WECK VISTA

GUDID 10886874112530

Laparoscopic trocar blade, single-use

Primary Device ID	10886874112530
NIH Device Record Key	949f703d-93aa-4018-8ef6-dce536ee847b
Commercial Distribution Status	In Commercial Distribution
Brand Name	WECK VISTA
Version Model Number	470360
Company DUNS	938647021
Company Name	INTUITIVE SURGICAL, 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	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	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00886874112533 [Primary]
GS1	10886874112530 [Package] Contains: 00886874112533 Package: BOX [6 Units] In Commercial Distribution
GS1	30886874112534 [Package] Package: CASE [5 Units] In Commercial Distribution

GCJ	Laparoscope, general & plastic surgery

Steralize Prior To Use	false
Device Is Sterile	true

10886874112691	STAPLER BLADELESS OBTURATOR, LONG
30886874112688	STAPLER BLADELESS OBTURATOR
10886874112530	BLADELESS OBTURATOR, LONG
10886874112523	BLADELESS OBTURATOR

Mark Image Registration \| Serial	Company Trademark Application Date
WECK VISTA 85474995 4310005 Live/Registered	Teleflex Incorporated 2011-11-17