Anesth ID Set Coax WT GSL 210 (BK OD22)

GUDID 04048675716273

Drägerwerk AG & Co. KGaA

Anaesthesia breathing circuit, single-use

• Primary Device ID: 04048675716273
• NIH Device Record Key: d38e1736-6688-4476-9a2d-9090ba2ad25f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Anesth ID Set Coax WT GSL 210 (BK OD22)
• Version Model Number: MP16052
• Company DUNS: 315578914
• Company Name: Drägerwerk AG & Co. KGaA
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048675716273 [Primary]

FDA Product Code

• CAI: Circuit, Breathing (W Connector, Adaptor, Y Piece)

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-21
• Device Publish Date: 2023-04-13

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