WECK VISTA

GUDID 10886874112691

STAPLER BLADELESS OBTURATOR, LONG

INTUITIVE SURGICAL, INC.

Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use Laparoscopic trocar blade, single-use

• Primary Device ID: 10886874112691
• NIH Device Record Key: 87781ab9-df75-43b3-b9ab-7183e16934b1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WECK VISTA
• Version Model Number: 470404
• 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 Dimensions

• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886874112694 [Primary]
GS1	10886874112691 [Package]; Contains: 00886874112694; Package: BOX [6 Units]; In Commercial Distribution
GS1	30886874112695 [Package]; Package: CASE [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K152663

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-03-02
• Device Publish Date: 2016-12-16

On-Brand Devices [WECK VISTA]

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