ENDOLOCK 13-1301I

GUDID 04250302201469

Fenestrated grasping forceps, 5 mm

Ackermann Instrumente GmbH

Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

• Primary Device ID: 04250302201469
• NIH Device Record Key: 0fdde4b9-cdba-4391-a229-4e21a7f8b352
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ENDOLOCK
• Version Model Number: 13-1301I
• Catalog Number: 13-1301I
• Company DUNS: 315121009
• Company Name: Ackermann Instrumente GmbH
• 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: 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: +497461966170
• Email: info@ackermanninstrumente.de

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250302201469 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K974382

FDA Product Code

• GCJ: Laparoscope, General & Plastic Surgery

Sterilization

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

[04250302201469]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-02-14

On-Brand Devices [ENDOLOCK]

• 04250302251372: Strong curved dissection forceps
• 04250302201469: Fenestrated grasping forceps, 5 mm
• 04250302200004: Tumor grasper, 5 mm, blunt end