MICASEPT PULMONALIS CLAMP

GUDID B09920919350040

MICASEPT PULMONALIS CLAMP HEGAR RATCHET CURVED LEFT CURVED DOWN

SONTEC INSTRUMENTS, INC.

Rigid endoscopic grasping forceps, reusable

• Primary Device ID: B09920919350040
• NIH Device Record Key: d337e450-f6c3-4629-9782-adbdda867b37
• Commercial Distribution Discontinuation: 2018-06-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MICASEPT PULMONALIS CLAMP
• Version Model Number: 20919-35-004
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B09920919350040 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K002877

FDA Product Code

• GCJ: Laparoscope, General & Plastic Surgery

Sterilization

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

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919350040]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

On-Brand Devices [MICASEPT PULMONALIS CLAMP ]

• B09920919340040: MICASEPT PULMONALIS CLAMP WITH HEGAR RATCHET CURVED RIGHT CURVED DOWN
• B09920919350040: MICASEPT PULMONALIS CLAMP HEGAR RATCHET CURVED LEFT CURVED DOWN
• B09920919340: MICASEPT PULMONALIS CLAMP ROUND RATCHET CURVED RIGHT CURVED DOWN
• 00192896115477: Micasept Pulmonalis Clamp With Round Ratchet 30 Degrees Curved Down Right