Boot Pad for Levitator Stirrup II, Regular, Right Leg 18-070-41

GUDID 04946329378238

Boot Pad for Levitator Stirrup II, Regular, Right Leg

MIZUHO CORPORATION

Leg procedure positioner

• Primary Device ID: 04946329378238
• NIH Device Record Key: 6f4ef46d-a823-403e-9e16-ef65718bc0f3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Boot Pad for Levitator Stirrup II, Regular, Right Leg
• Version Model Number: 18-070-41
• Catalog Number: 18-070-41
• Company DUNS: 690677802
• Company Name: MIZUHO CORPORATION
• 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: 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: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp

Device Dimensions

• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter
• Length: 363 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04946329378238 [Primary]

FDA Product Code

• GDC: Table, Operating-Room, Electrical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-30
• Device Publish Date: 2023-10-20

Devices Manufactured by MIZUHO CORPORATION

• 04946329416725 - SUGITA TITANIUM ANEURYSM CLIP II: 2025-05-05 TYPE: STANDARD, PERMANENT, No.V00 RANGE: 158-182gf(1.55-1.78N) MATERIAL: ISO 5832-3/ASTM F136, ISO 5832-2/ASTM F1341G2 BLADE: T-
• 04946329416732 - SUGITA TITANIUM ANEURYSM CLIP II: 2025-05-05 TYPE: STANDARD, PERMANENT, No.V01 RANGE: 158-182gf(1.55-1.78N) MATERIAL: ISO 5832-3/ASTM F136, ISO 5832-2/ASTM F1341G2 BLADE: T-
• 04946329416749 - SUGITA TITANIUM ANEURYSM CLIP II: 2025-05-05 TYPE: STANDARD, PERMANENT, No.V02 RANGE: 158-182gf(1.55-1.78N) MATERIAL: ISO 5832-3/ASTM F136, ISO 5832-2/ASTM F1341G2 BLADE: T-
• 04946329416756 - SUGITA TITANIUM ANEURYSM CLIP II: 2025-05-05 TYPE: STANDARD, PERMANENT, No.V03 RANGE: 158-182gf(1.55-1.78N) MATERIAL: ISO 5832-3/ASTM F136, ISO 5832-2/ASTM F1341G2 BLADE: T-
• 04946329416763 - SUGITA TITANIUM ANEURYSM CLIP II: 2025-05-05 TYPE: STANDARD, PERMANENT, No.V04 RANGE: 158-182gf(1.55-1.78N) MATERIAL: ISO 5832-3/ASTM F136, ISO 5832-2/ASTM F1341G2 BLADE: T-
• 04946329385519 - Operating Table MOT-VS700: 2024-11-14 SUSANO Pad for Back Section Type A
• 04946329385526 - Operating Table MOT-VS700: 2024-11-14 SUSANO Pad for Seat Section Type A
• 04946329385533 - Operating Table MOT-VS700: 2024-11-14 SUSANO Pad for Seat Section Type B