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US
Last updated May 27, 2026
What Molecular Products US Holdings, Inc. makes
The company produces carbon dioxide absorbent products designed for medical use, including canister packs and bulk pail formulations. These devices are intended for use in anesthesia workstations and respiratory equipment to absorb exhaled CO₂ during procedures. The products feature water-vapor indicating technology to monitor moisture levels and are available in standardized sizes for clinical settings.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates within the United States, adhering to applicable medical device compliance requirements for low-risk products.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Molecular Products US Holdings, Inc. manufacture?
Molecular Products US Holdings, Inc. specializes in carbon dioxide absorbent devices. These products are designed to absorb exhaled carbon dioxide during medical procedures, primarily used in anesthesia workstations and respiratory equipment. Examples include canister packs and bulk pail formulations, often featuring water-vapor indicating technology to monitor moisture levels.
Where is Molecular Products US Holdings, Inc. based?
The company is based in the United States. Its operations and manufacturing align with U.S. regulatory standards for medical devices, particularly those classified as low-risk.
Which regulatory registries list the devices produced by Molecular Products US Holdings, Inc.?
The devices manufactured by Molecular Products US Holdings, Inc. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring traceability and compliance.
How are the devices produced by Molecular Products US Holdings, Inc. classified under FDA regulations?
The company’s carbon dioxide absorbent devices fall under Class I classification by the FDA. This classification applies to low-risk medical devices that pose minimal potential harm to patients, requiring less stringent regulatory oversight compared to higher-risk categories.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 117988954
Catalogue (4)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Sodasorb® HMED, 4-8, W-V Indicating, Pail (17 kg), Smiths Medical 008880 | CD02-0007 | FDA UDI | Class I | Active |
| Sodasorb® HMED, 4-8, W-V Indicating, Pail (17 kg) | CD02-0004 | FDA UDI | Class I | Active |
| Sodasorb® HMED, 4-8, W-V Indicating, Individual Canister Pak, Smiths Medical 008 | CD02-0006 | FDA UDI | Class I | Active |
| Sodasorb® HMED, 4-8, W-V Indicating, Individual Canister Pak | CD02-0001 | FDA UDI | Class I | Active |
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