AED FB3954 Flexible Biopsy Cup w/ Teeth Forceps, 1.6mm x 220cm, 5FR FB3954

GUDID 00848657075114

A flexible, manual, non-electrosurgical instrument intended to obtain tissue specimens during endoscopic procedures (e.g., gastro-urological endoscopy, laparoscopy, bronchoscopy, laryngoscopy) for histopathological examination. It is typically a flexible metal coil with a pair of scissors-like cups with cutting edge rims, which are operated by a control handle at the proximal end of the instrument.

NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.

Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable

• Primary Device ID: 00848657075114
• NIH Device Record Key: 829d49e7-ce55-4d37-b9b1-d61997000cd3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AED FB3954 Flexible Biopsy Cup w/ Teeth Forceps, 1.6mm x 220cm, 5FR
• Version Model Number: FB3954
• Catalog Number: FB3954
• 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: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md
• Phone: +8182272720
• Email: customerservice@aed.md

Device Identifiers

Device Issuing Agency	Device ID
GS1	00848657075114 [Primary]

FDA Product Code

• KAE: Forceps, Ent

Sterilization

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

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

[00848657075114]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-05-26
• Device Publish Date: 2023-05-18

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