VersaGrasp Single use Grasping Forceps M0067802000

GUDID 16948318996794

VersaGrasp Single use Grasping Forceps

Anrei Medical(HZ) Co.,Ltd.

Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use

• Primary Device ID: 16948318996794
• NIH Device Record Key: b0c351fa-848b-4206-871d-5bddc876274a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VersaGrasp Single use Grasping Forceps
• Version Model Number: M0067802000
• Catalog Number: M0067802000
• Company DUNS: 529128653
• Company Name: Anrei Medical(HZ) Co.,Ltd.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06948318996797 [Primary]
GS1	16948318996794 [Package]; Contains: 06948318996797; Package: box [5 Units]; In Commercial Distribution

FDA Product Code

• PTS: Endoscopic Grasping/Cutting Instrument, Non-Powered, Exempt

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-24
• Device Publish Date: 2023-11-16

On-Brand Devices [VersaGrasp Single use Grasping Forceps]

• 06948318996094: This instrument has been designed to be used with an endoscope to retrieve foreign bodies or res
• 16948318996794: VersaGrasp Single use Grasping Forceps