Screwdriver, short 33000690

GUDID EBRE330006909

Screwdriver, short 1 Piece

bredent GmbH & Co. KG

Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable

• Primary Device ID: EBRE330006909
• NIH Device Record Key: 01954dff-8b58-41b8-9ce2-5cafd6da946b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Screwdriver, short
• Version Model Number: 33000690
• Catalog Number: 33000690
• Company DUNS: 341086190
• Company Name: bredent GmbH & Co. KG
• 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: true
• 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: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com
• Phone: +4907309872451
• Email: info@bredent.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry
• Special Storage Condition, Specify: Between 0 and 0 *keep dry

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EBRE330006900 [Primary]
HIBCC	EBRE330006909 [Package]; Contains: EBRE330006900; Package: dummy [1 Units]; Discontinued: 2023-09-22; Not in Commercial Distribution

FDA Product Code

• DZA: DRILL, DENTAL, INTRAORAL

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: 2023-10-02
• Device Publish Date: 2023-09-22

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