IVES-FANSLER RECTAL SPECULUM 90-0180

GUDID 00192896087941

IVES-FANSLER RECTAL SPECULUM WITH RUBBER OBTURATOR FENESTRATED HANDLE

SONTEC INSTRUMENTS, INC.

Rectal speculum

• Primary Device ID: 00192896087941
• NIH Device Record Key: 4390de70-470b-48d0-b833-8c416f7a96e8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IVES-FANSLER RECTAL SPECULUM
• Version Model Number: 90-0180
• Catalog Number: 90-0180
• 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	00192896087941 [Primary]

FDA Product Code

• FFQ: SPECULUM, RECTAL

Sterilization

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

[00192896087941]

Dry Heat Sterilization;Moist Heat or Steam 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 [IVES-FANSLER RECTAL SPECULUM]

• 00192896087941: IVES-FANSLER RECTAL SPECULUM WITH RUBBER OBTURATOR FENESTRATED HANDLE
• 00192896075337: IVES-FANSLER RECTAL SPECULUM LONG CHROME HANDLE