AUFRICHT RETRACTOR 207-292

GUDID 00192896025660

AUFRICHT RETRACTOR SOLID BLADE

SONTEC INSTRUMENTS, INC.

Hand-held surgical retractor, reusable

• Primary Device ID: 00192896025660
• NIH Device Record Key: db897f69-fd29-4478-829f-837c5ba91672
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AUFRICHT RETRACTOR
• Version Model Number: 207-292
• Catalog Number: 207-292
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896025660 [Primary]

FDA Product Code

• GAD: RETRACTOR
• KAL: Retractor, Ent

Sterilization

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

[00192896025660]

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: 2019-11-19
• Device Publish Date: 2018-09-11

On-Brand Devices [AUFRICHT RETRACTOR]

• 00192896090330: AUFRICHT RETRACTOR SOLID BLADE
• 00192896025745: AUFRICHT RETRACTOR SOLID BLADE BLACK NON-REFLECTIVE FINISH
• 00192896025738: AUFRICHT RETRACTOR ILLUMINATED SOLID BLADE
• 00192896025660: AUFRICHT RETRACTOR SOLID BLADE
• 00192896025653: AUFRICHT RETRACTOR FENESTRATED BLADE
• 00192896116009: Aufricht Nasal Retractor Illuminated