EXMOOR S101

GUDID 05060180250232

Suction Tube

EXMOOR PLASTICS LIMITED

Surgical/emergency suction cannula, non-illuminating, single-use

• Primary Device ID: 05060180250232
• NIH Device Record Key: 396349d2-a480-47d7-afed-e0c7d07eeddd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EXMOOR
• Version Model Number: S101
• Catalog Number: S101
• Company DUNS: 298725490
• Company Name: EXMOOR PLASTICS LIMITED
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +441823351040
• Email: sales@exmoorltd.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *store in clean, dry environment at room temperature, avoid extremes of temperature and humidity.
• Special Storage Condition, Specify: Between 0 and 0 *store in clean, dry environment at room temperature, avoid extremes of temperature and humidity.
• Special Storage Condition, Specify: Between 0 and 0 *store in clean, dry environment at room temperature, avoid extremes of temperature and humidity.
• Special Storage Condition, Specify: Between 0 and 0 *store in clean, dry environment at room temperature, avoid extremes of temperature and humidity.

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060180250232 [Package]; Contains: 05060180257798; Package: A BOX [50 Units]; In Commercial Distribution
GS1	05060180257798 [Primary]

FDA Product Code

• JZF: Tube, Ear Suction

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-04-20
• Device Publish Date: 2018-09-11

On-Brand Devices [EXMOOR]

• 05060180254896: Laryngeal Suction Tube
• 05060180253653: Myringotomy Kit with Grommets
• 05060180259242: Silicone packing strip
• 05060180255213: Silicone Tooth Protector
• 05060180255176: Myringotomy Kit
• 05060180255152: Silicone packing strip
• 05060180253646: Myringotomy Kit with Grommets
• 05060180250904: Myringotomy Kit with Grommets
• 05060180255008: Myringotomy Kit
• 05060180254919: Laryngeal Suction Tube
• 05060180250898: Myringotomy Kit with Grommets
• 05060180250881: Myringotomy Kit with Grommets
• 05060180254797: Laryngeal Suction Tube
• 05060180254780: Laryngeal Suction Tube
• 05060180254773: Laryngeal Suction Tube
• 05060180254759: Laryngeal Suction Tube
• 05060180250874: Myringotomy Kit with Grommets
• 05060180250867: Myringotomy Kit with Grommets
• 05060180250850: Myringotomy Kit with Grommets
• 05060180250843: Myringotomy Kit with Grommets
• 05060180250836: Myringotomy Kit with Grommets
• 05060180252120: Epidrum
• 05060180252113: Epidrum
• 05060180254483: Economy Kit
• 05060180254582: Myringotomy Kit
• 05060180250829: Myringotomy Kit with Grommets
• 05060180253158: Mal Ear Mop
• 05060180254391: Suction Tube
• 05060180254384: Suction Tube
• 05060180254377: Suction Tube
• 05060180254360: Suction Tube
• 05060180254353: Suction Tube
• 05060180254346: Suction Tube
• 05060180254339: Suction Tube
• 05060180254322: Suction Tube
• 05060180254315: Suction Tube
• 05060180254308: Suction Tube
• 05060180254292: Suction Tube
• 05060180250188: Suction Tube
• 05060180250225: Suction Tube
• 05060180250218: Suction Tube
• 05060180250201: Suction Tube
• 05060180250195: Suction Tube
• 05060180254285: Suction Tube
• 05060180254278: Suction Tube
• 05060180254261: Suction Tube
• 05060180254254: Suction Tube
• 05060180254247: Suction Tube
• 05060180254230: Suction Tube
• 05060180254223: Suction Tube