Anesthesia Set Flex Latex

GUDID 04048675028826

Drägerwerk AG & Co. KGaA

Anaesthesia breathing circuit, single-use

• Primary Device ID: 04048675028826
• NIH Device Record Key: 6eb5c70e-e667-4369-9045-1f4e17d5d45f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Anesthesia Set Flex Latex
• Version Model Number: MP00304
• Company DUNS: 315578914
• Company Name: Drägerwerk AG & Co. KGaA
• Device Count: 25
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +494518820
• Email: [email protected]

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048675028826 [Primary]
GS1	04048675422419 [Unit of Use]

FDA Product Code

• BTC: Bag, Reservoir

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-11-27
• Device Publish Date: 2015-10-24

Devices Manufactured by Drägerwerk AG & Co. KGaA

• 04048675253372 - VentStar Helix heated: 2019-11-27
• 04048675253365 - VentStar Helix dual heated: 2019-11-27
• 04048675253358 - AutoFeed Chamber: 2019-11-27
• 04048675252023 - VentStar Anesthesia Basic 250: 2019-11-27
• 04048675252016 - VentStar Anesthesia Basic 180: 2019-11-27
• 04048675251903 - VentStar Basic(P)250: 2019-11-27
• 04048675251538 - VentStar Anesth WT(P) 180 w/oLL: 2019-11-27
• 04048675251521 - VentStar Anesthesia WT (P)180: 2019-11-27