GUBISCH AUFRICHT NASAL RETRACTOR 207-2922

GUDID 00192896025684

G. AUFRICHT NASAL RETRACTOR SOLID TAPERED BLADE

SONTEC INSTRUMENTS, INC.

Hand-held surgical retractor, reusable

• Primary Device ID: 00192896025684
• NIH Device Record Key: 6fcbe698-53f8-417a-8362-d24dc2d725bd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GUBISCH AUFRICHT NASAL RETRACTOR
• Version Model Number: 207-2922
• Catalog Number: 207-2922
• 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: 6.75 Inch
• Length: 6.75 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896025684 [Primary]

FDA Product Code

• KAL: RETRACTOR, ENT

Sterilization

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

[00192896025684]

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: 2019-11-20
• Device Publish Date: 2018-09-11

On-Brand Devices [GUBISCH AUFRICHT NASAL RETRACTOR]

• 00192896090323: G. AUFRICHT NASAL RETRACTOR SOLID TAPERED BLADE
• 00192896025684: G. AUFRICHT NASAL RETRACTOR SOLID TAPERED BLADE
• 00192896025677: G. AUFRICHT NASAL RETRACTOR SOLID TAPERED BLADE