SCOPE BUDDY ADAPTER

GUDID 00677964056246

MEDIVATORS INC.

Luer/non-ISO80369-standardized linear connector, reusable

• Primary Device ID: 00677964056246
• NIH Device Record Key: 1207bfc7-7093-4cc3-bc00-151fe6424b93
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCOPE BUDDY ADAPTER
• Version Model Number: SB-110-HU1005
• Company DUNS: 068199363
• Company Name: MEDIVATORS INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: 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

Customer Support Contacts

• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com
• Phone: +1(800)444-4729
• Email: custserv@MEDIVATORS.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00677964056246 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162128

FDA Product Code

• FEB: Accessories, Cleaning, For Endoscope

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-10-23
• Device Publish Date: 2019-10-10

Devices Manufactured by MEDIVATORS INC.

• 50677964151335 - Endo Carry-on Procedure Kit: 2025-08-25 Endo Carry-on Procedure Kit contains Basin, VIA Sponge, Defendo Fuji 700 5-Piece Kit, Absorbant Pad, Lubricant, Gauze, and DuoSw
• 50677964151342 - Endo Carry-on Procedure Kit: 2025-08-25 Endo Carry-on Procedure Kit contains Revital Ox Bedside Concentrate, Defendo Olympus 5-Piece Kit, Drawstring Pad, Absorbant Pads
• 50677964151359 - Endo Carry-on Procedure Kit: 2025-08-25 Endo Carry-on Procedure Kit contains Basin, VIA Enzymatic Sponge, Defendo Olympus 4-Piece Kit, Cleanascope Advantage Liners, Abs
• 50677964151366 - Endo Carry-on Procedure Kit: 2025-08-25 Endo Carry-on Procedure Kit contains Intercept Bedside Kit, Defendo Olympus 5-Piece Kit, Drawstring Pad, Extra Absorbant Pad, Lu
• 50677964151373 - Endo Carry-on Procedure Kit: 2025-08-25 Endo Carry-on Procedure Kit contains Basin, Defendo Olympus 5-Piece Kit, Transport Pad, Lubricant, Gauze, and Biohazard Sticker.
• 50677964151380 - Endo Carry-on Procedure Kit: 2025-08-25 Endo Carry-on Procedure Kit contains Intercept Bedside Kit, Defendo Olympus 5-Piece Kit, Take-Out Transport Pad, Lubricant, Gauz
• 50677964151397 - Endo Carry-on Procedure Kit: 2025-08-25 Endo Carry-on Procedure Kit contains Intercept Detergent Packet, Flat Sponge, Cylindrical Sponge, STERIS Fuji 700 4-Piece Kit, D
• 50677964151403 - Endo Carry-on Procedure Kit: 2025-08-25 Endo Carry-on Procedure Kit contains Intercept Bedside Complete Kit, Defendo Olympus 5-Piece Kit, Drawstring Pad, Lubricant, Gau