Cup Biopsy, Double Action 86422430

GUDID 00848657075220

A semi-rigid forcep inserted through the working channel of an endoscope to grasp tissue or other foreign bodies. It has a leur port for cleaning.

NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.

Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable Flexible endoscopic tissue manipulation forceps, reusable

• Primary Device ID: 00848657075220
• NIH Device Record Key: 947b3bad-fc87-42b5-a60f-53559d187f2e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cup Biopsy, Double Action
• Version Model Number: 86422430
• Catalog Number: 86422430
• Company DUNS: 839138955
• Company Name: NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
• 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

Customer Support Contacts

• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md
• Phone: (818) 227-2720
• Email: customerservice@aed.md

Device Identifiers

Device Issuing Agency	Device ID
GS1	00848657075220 [Primary]

FDA Product Code

• HIH: Hysteroscope (And Accessories)

Sterilization

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

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

[00848657075220]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-10-06
• Device Publish Date: 2021-09-28

Devices Manufactured by NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.

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• 00848657076807 - Rat Tooth Grasper, D/A, Rotating, 3mm x 37cm: 2024-07-10 A flexible, hand-held manual surgical instrument designed to be introduced through the working channel of an endoscope to grasp
• 00848657076814 - Curved Metz Scissor, D/A, Rotating, 3mm x 37cm: 2024-07-10 A flexible, hand-held manual surgical instrument designed to be introduced through the working channel of an endoscope to grasp
• 00848657076821 - Large Biopsy Cup Forcep, D/A, 3mm x 37cm: 2024-07-10 A flexible, manual, non-electrosurgical instrument intended to obtain tissue specimens during endoscopic procedures (e.g., gastr
• 00848657076920 - ENDOPRO-CAM Master Series: 2024-06-19 Endoscopic Video System
• 00848657076937 - ENDOPRO-MDTK: 2024-06-19 Monostereo 3D Video System Enhancement
• 00848657023108 - AED Power Bank Battery, Rechargeable: 2023-10-20 AED Power Bank Battery, Rechargeable
• 00848657068796 - Retractor: 2023-10-20 A hand-held, non-self-retaining surgical instrument intended to be used to separate/draw aside the margins of a wound/incision t