LATEX O-RINGS

GUDID B0995085520

LATEX O-RINGS SMALL (100 PER BAG)

SONTEC INSTRUMENTS, INC.

Haemorrhoid ligator

• Primary Device ID: B0995085520
• NIH Device Record Key: 7d8b150e-ded6-4b59-9249-5aedfefba409
• Commercial Distribution Discontinuation: 2018-09-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: LATEX O-RINGS
• Version Model Number: 508-552
• 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: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B0995085520 [Primary]

FDA Product Code

• FHN: Ligator, Hemorrhoidal

Sterilization

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

[B0995085520]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0995085520]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 7
• Public Version Date: 2018-09-24
• Device Publish Date: 2016-08-19

On-Brand Devices [LATEX O-RINGS ]

• B0995085510: LATEX O-RINGS REGULAR (100 PER BAG)
• B0995085520: LATEX O-RINGS SMALL (100 PER BAG)