Screw Driver ASCSD30

GUDID 08800292999295

Megagen Implant Co. Ltd

Surgical screwdriver, reusable

• Primary Device ID: 08800292999295
• NIH Device Record Key: aa02b01e-1612-4d83-ad54-ee6a16d2e9e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Screw Driver
• Version Model Number: ASCSD30
• Catalog Number: ASCSD30
• Company DUNS: 687388178
• Company Name: Megagen Implant Co. Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800292999295 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800292999295]

Moist Heat or Steam Sterilization

[08800292999295]

Moist Heat or Steam Sterilization

[08800292999295]

Moist Heat or Steam Sterilization

[08800292999295]

Moist Heat or Steam Sterilization

[08800292999295]

Moist Heat or Steam Sterilization

[08800292999295]

Moist Heat or Steam Sterilization

[08800292999295]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-30
• Device Publish Date: 2026-03-20

On-Brand Devices [Screw Driver]

• 08800292999295: ASCSD30
• 08800292999288: ASCSD25
• 08800292999271: ASCSD20
• 08800292999264: ASCSD15