485 KIT

GUDID 08809917165459

Osstem Implant Co., Ltd.

Dental/maxillofacial surgical procedure kit, non-medicated, reusable

• Primary Device ID: 08809917165459
• NIH Device Record Key: d93aa66a-8ef7-4f54-8745-12d1de7b0f24
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 485 KIT
• Version Model Number: HK485K
• Company DUNS: 689051793
• Company Name: Osstem Implant Co., Ltd.
• 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: true
• Device Combination Product: false
• Single Use: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809917165459 [Primary]

FDA Product Code

• NYE: Fixture Mount Kit

Sterilization

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

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

[08809917165459]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-29
• Device Publish Date: 2024-04-19

On-Brand Devices [485 KIT]

• 08800121792820: H485K
• 08800040606604: O485K
• 08809917165459: HK485K
• 08809917070067: O485K
• 08800271260309: HK485K