MEEKER HEMOSTATIC FORCEPS 2200-440

GUDID 00192896060913

MEEKER HEMOSTATIC FORCEPS RIGHT ANGLE CURVED TIP

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable

• Primary Device ID: 00192896060913
• NIH Device Record Key: dddc5d21-d345-4fca-bc33-528f498fc2e6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEEKER HEMOSTATIC FORCEPS
• Version Model Number: 2200-440
• Catalog Number: 2200-440
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• 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: 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: +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
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896060913 [Primary]

FDA Product Code

• HRQ: Hemostat
• HTD: FORCEPS

Sterilization

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

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896060913]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-21
• Device Publish Date: 2018-10-04

On-Brand Devices [MEEKER HEMOSTATIC FORCEPS]

• 00192896060913: MEEKER HEMOSTATIC FORCEPS RIGHT ANGLE CURVED TIP
• 00192896117129: Meeker Hemostatic Forceps Quantum