Unimicro

GUDID 16955797740022

Veress needle

Unimicro Medical Systems (ShenZhen) Co., Ltd.

Spring-loaded pneumoperitoneum needle, single-use

• Primary Device ID: 16955797740022
• NIH Device Record Key: f895543c-6458-4dab-8d92-33aa1351b4db
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Unimicro
• Version Model Number: MND11500
• Company DUNS: 421327368
• Company Name: Unimicro Medical Systems (ShenZhen) Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06955797740025 [Primary]
GS1	16955797740022 [Package]; Contains: 06955797740025; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• FHO: Pneumoperitoneum Needle

Sterilization

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

[16955797740022]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-12-22

On-Brand Devices [Unimicro ]

• 16955797740022: Veress needle
• 16955797740015: Veress needle