Paper-Forceps curved

GUDID E210BK1330

Dr. Jean Bausch GmbH & Co. KG

Dental articulation paper forceps

• Primary Device ID: E210BK1330
• NIH Device Record Key: 8f145a4b-f257-436d-aacf-fceff96e453c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Paper-Forceps curved
• Version Model Number: BK 133
• Company DUNS: 321624272
• Company Name: Dr. Jean Bausch 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E210BK1330 [Primary]

FDA Product Code

• EFK: Forceps, Articulation Paper

Sterilization

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

[E210BK1330]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-01-13
• Device Publish Date: 2020-01-03

Devices Manufactured by Dr. Jean Bausch GmbH & Co. KG

• E210BK1330 - Paper-Forceps curved: 2020-01-13
• E210BK1330 - Paper-Forceps curved: 2020-01-13
• E210BK1420 - Articulating Paper Forceps "Miller": 2020-01-13
• E210BK1430 - FIX-CLIP: 2020-01-13
• E210BK1440 - Arti-Fol®-Forceps "SteriSlide": 2020-01-13
• E210BK1450 - Arti-Fol® Approximal Contact Forceps: 2020-01-13
• E210BK13209 - Arti-Fol®-Forceps straight, longitudinal groove: 2019-12-30
• E210BK14008 - Bausch Y-Holder: 2019-12-30