STERLING

GUDID 00366975023520

#32 STERLING™ Extracting Serrated Forcep

BENCO DENTAL SUPPLY CO.

Tooth extraction forceps

• Primary Device ID: 00366975023520
• NIH Device Record Key: 055de09d-3554-47bb-8358-8f53a384a4e0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STERLING
• Version Model Number: 4031-932
• Company DUNS: 015108087
• Company Name: BENCO DENTAL SUPPLY CO.
• 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: 570-602-6924
• Email: jsoroka@benco.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Instruments should be stored dry, dust-free and away from chemical products. Avoid temperature fluctuations and direct sunlight, Take measures to product against damage during transport and storage.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00366975023520 [Primary]

FDA Product Code

• EMG: Forceps, Tooth Extractor, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-22
• Device Publish Date: 2018-09-21

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