Surgical Guide Bone Pusher

GUDID 08800039301251

InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)

Fixture/appliance dental drill bit, reusable Fixture/appliance dental drill bit, reusable Fixture/appliance dental drill bit, reusable Fixture/appliance dental drill bit, reusable Fixture/appliance dental drill bit, reusable

• Primary Device ID: 08800039301251
• NIH Device Record Key: b0fa9eb4-7da0-430d-b807-c576ca9482c4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Surgical Guide Bone Pusher
• Version Model Number: MSBP
• Company DUNS: 631169224
• Company Name: InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• 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: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800039301251 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800039301251]

Moist Heat or Steam Sterilization

[08800039301251]

Moist Heat or Steam Sterilization

[08800039301251]

Moist Heat or Steam Sterilization

[08800039301251]

Moist Heat or Steam Sterilization

[08800039301251]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-26
• Device Publish Date: 2022-05-18

On-Brand Devices [Surgical Guide Bone Pusher]

• 08800039301251: MSBP
• 08800039301244: FSBP