AUT179095PF-3

GUDID 20888551044261

Versaport V2 11mm Trocar with Fixation Cannula and Universal Seal 3/bx

STERILMED, INC.

Laparoscopic trocar blade, reprocessed

• Primary Device ID: 20888551044261
• NIH Device Record Key: 799b1647-bc8c-4fba-8eb2-819bcca6f388
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: AUT179095PF-3
• Catalog Number: AUT179095PF-3
• Company DUNS: 175899459
• Company Name: STERILMED, 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: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(888)541-0078
• Email: customerservice@sterilmed.com
• Phone: +1(888)541-0078
• Email: customerservice@sterilmed.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	20888551044261 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K012578

FDA Product Code

• NLM: LAPAROSCOPE, GENERAL & PLASTIC SURGERY, REPROCESSED

Sterilization

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

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

[20888551044261]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-22

Devices Manufactured by STERILMED, INC.

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• 10888551045186 - NA: 2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
• 10888551045193 - NA: 2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, F CURVE
• 10888551045209 - NA: 2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
• 10888551010313 - NA: 2021-01-22 KNIFE SET ECTRA II (PACK OF 3)
• 10888551021531 - NA: 2021-01-22 KNIVES (1) HOOK BLADE (1) TRIANGLE BLADE ENDOTRAC BLADE SYSTEM
• 10888551000048 - NA: 2020-11-06 CTS RELIEF KIT, 5PC SET
• 10888551012928 - NA: 2020-10-19 ENDO LUNG