MICASEPT DEBAKEY ORGAN GRASPING FORCEPS

GUDID B09920919050550

MICASEPT DEBAKEY ORGAN GRASPING FORCEPS FOLDING RATCHET OPENING DOWN ANGLED

SONTEC INSTRUMENTS, INC.

Rigid endoscopic grasping forceps, reusable Rigid endoscopic grasping forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable

• Primary Device ID: B09920919050550
• NIH Device Record Key: c0fe92f3-8b4f-4b1f-8514-0947f5606c05
• Commercial Distribution Discontinuation: 2018-06-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MICASEPT DEBAKEY ORGAN GRASPING FORCEPS
• Version Model Number: 20919-05-055
• 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
• 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
• 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	B09920919050550 [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

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919050550]

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 DEBAKEY ORGAN GRASPING FORCEPS]

• B09920919050600: MICASEPT DEBAKEY ORGAN GRASPING FORCEPS ROUND RATCHET OPENING DOWN ANGLED
• B09920919053040: MICASEPT DEBAKEY ORGAN GRASPING FORCEPS WITH HEGAR RATCHET STRAIGHT
• B09920919050640: MICASEPT DEBAKEY ORGAN GRASPING FORCEPS WITH HEGAR RATCHET DOWN ANGLED OPENING
• B09920919050440: MICASEPT DEBAKEY ORGAN GRASPING FORCEPS WITH HEGAR RATCHET DOWN ANGLED OPENING
• B09920919050400: MICASEPT DEBAKEY ORGAN GRASPING FORCEPS WITH ROUND RATCHET DOWN ANGLED OPENING
• B09920919050650: MICASEPT DEBAKEY ORGAN GRASPING FORCEPS FOLDING RATCHET OPENING DOWN ANGLED
• B09920919050550: MICASEPT DEBAKEY ORGAN GRASPING FORCEPS FOLDING RATCHET OPENING DOWN ANGLED