HYBRID HERBST WIRE PASSER 1103-1661

GUDID 00192896030565

HYBRID HERBST WIRE PASSER SINGLE ENDED TIP PHENOLIC HANDLE

SONTEC INSTRUMENTS, INC.

Wire/ligature passer, reusable

• Primary Device ID: 00192896030565
• NIH Device Record Key: beb83bfd-2751-4f90-a2bc-f4d86dbc76ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HYBRID HERBST WIRE PASSER
• Version Model Number: 1103-1661
• Catalog Number: 1103-1661
• 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

Device Dimensions

• Length: 10.5 Inch
• Length: 10.5 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896030565 [Primary]

FDA Product Code

• HXI: Passer, Wire, Orthopedic

Sterilization

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

[00192896030565]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-10-29
• Device Publish Date: 2018-09-20

On-Brand Devices [HYBRID HERBST WIRE PASSER]

• 00192896082694: HYBRID HERBST WIRE PASSER SINGLE ENDED TIP PHENOLIC HANDLE
• 00192896030565: HYBRID HERBST WIRE PASSER SINGLE ENDED TIP PHENOLIC HANDLE