MICASEPT CIRADUR BIOPSY FORCEPS 20934-01-300

GUDID 00192896008717

MICASEPT CIRADUR BIOPSY FORCEPS STRAIGHT

SONTEC INSTRUMENTS, INC.

Open-surgery biopsy forceps, reusable

• Primary Device ID: 00192896008717
• NIH Device Record Key: db707fd5-648f-4be9-9df0-e5c750e82ab6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICASEPT CIRADUR BIOPSY FORCEPS
• Version Model Number: 20934-01-300
• Catalog Number: 20934-01-300
• 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: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Outer Diameter: 4.5 Millimeter
• Outer Diameter: 4.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896008717 [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

[00192896008717]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-07-12
• Device Publish Date: 2018-08-15

On-Brand Devices [MICASEPT CIRADUR BIOPSY FORCEPS]

• 00192896008717: MICASEPT CIRADUR BIOPSY FORCEPS STRAIGHT
• B09920934010: MICASEPT CIRADUR BIOPSY FORCEPS CURVED DOWN