Unimax

GUDID 14714127866236

Monopolar Forceps

UNIMAX MEDICAL SYSTEMS INC.

Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

• Primary Device ID: 14714127866236
• NIH Device Record Key: bfa1da32-6329-464a-9ecb-6258c2db9e69
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Unimax
• Version Model Number: FEC533050
• Company DUNS: 658122465
• Company Name: UNIMAX MEDICAL SYSTEMS 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: 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04714127866239 [Primary]
GS1	14714127866236 [Package]; Contains: 04714127866239; Package: Paper Box [10 Units]; In Commercial Distribution
GS1	24714127866233 [Package]; Package: Carton [10 Units]; In Commercial Distribution

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2021-03-11
• Device Publish Date: 2021-03-03

On-Brand Devices [Unimax]

• 14714127866236: Monopolar Forceps
• 24714127866806: Monopolar spatula probe
• 24714127866707: Monopolar L hook probe
• 24714127866608: Monopolar J hook probe
• 14714127868711: Closed suction catheter
• 14714127868568: Closed suction catheter
• 14714127868551: Closed suction catheter
• 14714127863570: Detachable endo pocket