A200SP Absorber MRI

GUDID 05051977000109

Anaesthesia Absorber for use in MRI environment and all clinical environments.

PENLON LTD

Anaesthesia breathing circuit, reusable

• Primary Device ID: 05051977000109
• NIH Device Record Key: 3e211df9-d9da-4d5f-83fc-ebc830fec492
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A200SP Absorber MRI
• Version Model Number: A200SP
• Company DUNS: 458942687
• Company Name: PENLON LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• 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	05051977000109 [Primary]

FDA Product Code

• BSF: Absorber, Carbon-Dioxide

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-27

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