VERNON DAVID RECTAL SPECULUM 508-344

GUDID 00192896044517

VERNON-DAVID RECTAL SPECULUM SHORT TUBE GRIP HANDLE

SONTEC INSTRUMENTS, INC.

Rectal speculum

• Primary Device ID: 00192896044517
• NIH Device Record Key: 7293fb13-77f6-43e5-a2aa-c3ff73a3b48f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VERNON DAVID RECTAL SPECULUM
• Version Model Number: 508-344
• Catalog Number: 508-344
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00192896044517 [Primary]

FDA Product Code

• FFQ: SPECULUM, RECTAL

Sterilization

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

[00192896044517]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-18
• Device Publish Date: 2018-09-17

On-Brand Devices [VERNON DAVID RECTAL SPECULUM]

• 00192896044524: VERNON-DAVID RECTAL SPECULUM LONG TUBE GRIP HANDLE
• 00192896044517: VERNON-DAVID RECTAL SPECULUM SHORT TUBE GRIP HANDLE