Hobbs Medical Grasping Forceps Handle 5050

GUDID M84950500

A control handle for a flexible manual device intended to be used in combination with a compatible endoscope to grasp foreign bodies. The device is constructed of a flexible metal coil and plastic tube whose distal end is equipped with grasping tongs which are operated by a control handle attached at the proximal end of the instrument. It is introduced into the body cavity through the working channel of the endoscope. This is a reuseable device.

HOBBS MEDICAL, INC.

Flexible endoscopic tissue manipulation forceps, reusable

• Primary Device ID: M84950500
• NIH Device Record Key: 304ec61a-2778-4d59-8811-1b2523f89d32
• Commercial Distribution Discontinuation: 2025-11-21
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Hobbs Medical Grasping Forceps Handle
• Version Model Number: 5050
• Catalog Number: 5050
• Company DUNS: 076769355
• Company Name: HOBBS MEDICAL, 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M84950500 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K833125

FDA Product Code

• OCX: Endoscopic Irrigation/Suction System

Sterilization

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

[M84950500]

Liquid Chemical

[M84950500]

Liquid Chemical

[M84950500]

Liquid Chemical

[M84950500]

Liquid Chemical

[M84950500]

Liquid Chemical

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2025-11-24
• Device Publish Date: 2016-09-21

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