Bite Impression Coping (Mini)

GUDID 00810019244223

HIOSSEN, INC.

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 00810019244223
• NIH Device Record Key: b1baaa90-b970-4ed7-8afd-cc741e26f337
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bite Impression Coping (Mini)
• Version Model Number: ETBICM4430
• Company DUNS: 796083090
• Company Name: HIOSSEN, 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: true
• 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
GS1	00810019244223 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

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: 2021-08-04
• Device Publish Date: 2021-07-27

On-Brand Devices [Bite Impression Coping (Mini)]

• 00810019244353: ETBICM4651
• 00810019244346: ETBICM4650
• 00810019244339: ETBICM4641
• 00810019244322: ETBICM4640
• 00810019244315: ETBICM4631
• 00810019244308: ETBICM4630
• 00810019244292: ETBICM4621
• 00810019244285: ETBICM4620
• 00810019244278: ETBICM4451
• 00810019244261: ETBICM4450
• 00810019244254: ETBICM4441
• 00810019244247: ETBICM4440
• 00810019244230: ETBICM4431
• 00810019244223: ETBICM4430
• 00810019244216: ETBICM4421
• 00810019244209: ETBICM4420
• 00810019247835: EKBIC4641