SQ AXEL Countersink

GUDID 08800313230642

SQ AXEL Countersink (DSACS38)

DENTIS CO. ,LTD

Surgical countersink, reusable

• Primary Device ID: 08800313230642
• NIH Device Record Key: f695fc75-0a97-46d6-bc0b-93154bc13f6c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SQ AXEL Countersink
• Version Model Number: DSACS38
• Company DUNS: 694721181
• Company Name: DENTIS 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: 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	08800313230642 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800313230642]

Moist Heat or Steam Sterilization

[08800313230642]

Moist Heat or Steam Sterilization

[08800313230642]

Moist Heat or Steam Sterilization

[08800313230642]

Moist Heat or Steam Sterilization

[08800313230642]

Moist Heat or Steam Sterilization

[08800313230642]

Moist Heat or Steam Sterilization

[08800313230642]

Moist Heat or Steam Sterilization

[08800313230642]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-19
• Device Publish Date: 2026-03-11

On-Brand Devices [SQ AXEL Countersink]

• 08800313230673: SQ AXEL Countersink (DSACS50)
• 08800313230666: SQ AXEL Countersink (DSACS46)
• 08800313230659: SQ AXEL Countersink (DSACS42)
• 08800313230642: SQ AXEL Countersink (DSACS38)