Mediflex Deluxe Laparoscopic Instruments 91302-DR-RLF

GUDID 00842102105159

RELIEF Deluxe Maxi-Grip Fundus Grasper, 17mm, 5mm x 36cm

FLEXBAR MACHINE CORPORATION

Rigid endoscopic tissue manipulation forceps, reusable

• Primary Device ID: 00842102105159
• NIH Device Record Key: 62fdb8b7-f7a2-41e5-a381-5bdda8eac2ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mediflex Deluxe Laparoscopic Instruments
• Version Model Number: 91302-DR-RLF
• Catalog Number: 91302-DR-RLF
• Company DUNS: 047644935
• Company Name: FLEXBAR MACHINE CORPORATION
• 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: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842102105159 [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

[00842102105159]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-08-21
• Device Publish Date: 2017-02-15

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