BONE PROFILER SLEEVE A-PAD-GUI-PS-250

GUDID D7701352403

BONE PROFILER SLEEVE EX.2.50 MM

SWEDEN & MARTINA SPA

Dental implant/prosthesis surgical procedure kit

• Primary Device ID: D7701352403
• NIH Device Record Key: 08463582-74d4-4c2e-ac3c-9aa77cd15cf7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BONE PROFILER SLEEVE
• Version Model Number: A-PAD-GUI-PS-250
• Catalog Number: A-PAD-GUI-PS-250
• Company DUNS: 433815198
• Company Name: SWEDEN & MARTINA SPA
• Device Count: 1
• DM Exempt: true
• 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: true
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: 844.862.7846
• Email: info.us@sweden-martina.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7701352403 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[D7701352403]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-08-17
• Device Publish Date: 2018-07-17

On-Brand Devices [BONE PROFILER SLEEVE]

• D7701352403: BONE PROFILER SLEEVE EX.2.50 MM
• D7701352393: BONE PROFILER SLEEVE EX.2.30 MM
• D7702693393: BONE PROFILER SLEEVE 5.0