Ambia

GUDID 04048675595328

Drägerwerk AG & Co. KGaA

General utility supply system, ceiling-mounted

• Primary Device ID: 04048675595328
• NIH Device Record Key: fb948aa5-a395-4ed6-bd41-f06abb3f5e99
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ambia
• Version Model Number: GG16010
• Company DUNS: 315578914
• Company Name: Drägerwerk AG & Co. KGaA
• Device Count: 1
• 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: false
• Lot Batch: false
• 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	04048675595328 [Primary]

FDA Product Code

• FQO: Table, Operating-Room, Ac-Powered

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: 2021-10-14
• Device Publish Date: 2021-10-06

Devices Manufactured by Drägerwerk AG & Co. KGaA

• 04048675013532 - CORRUGATED BELLOWS K: 2026-02-03
• 04048675558736 - Filter SafeStar 55 Plus: 2026-01-23
• 04048675665762 - Filter SafeStar 90 Plus: 2026-01-23
• 04048675665786 - Filter SafeStar 60A Plus: 2026-01-23
• 04048675665823 - Filter/HME TwinStar HEPA Plus: 2026-01-23
• 04048675253426 - Mask NovaStarTS,NIV,w/SE,L: 2026-01-16
• 04048675253402 - Mask NovaStarTS,NIV,w/SE,S: 2026-01-16
• 04048675253419 - Mask NovaStarTS,NIV,w/SE,M: 2026-01-16