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Sign in to claim this brandVIACORD, LLC
US
Last updated May 23, 2026
What VIACORD, LLC makes
Viacord, LLC manufactures umbilical cord blood collection sets designed for the retrieval of stem cells from newborns during and immediately after childbirth. These kits are intended for use in private banking or research applications, ensuring the collection of cord blood in a sterile, controlled environment.
The company’s products are classified under the FDA’s Unique Device Identifier (UDI) system and fall within regulatory categories relevant to in vitro diagnostics and cellular therapy collection devices. Viacord, LLC is based in the United States.
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 Viacord, LLC manufacture?
Viacord, LLC specializes in umbilical cord blood collection sets. These devices are specifically designed to collect stem cells from the umbilical cord of newborns during or immediately after childbirth. The kits ensure a sterile and controlled collection process, primarily intended for private banking or research purposes.
Where is Viacord, LLC based?
Viacord, LLC is headquartered in the United States. The company’s location is relevant for regulatory compliance and reporting purposes, as it operates under the jurisdiction of the U.S. Food and Drug Administration (FDA).
Which regulatory registries or databases list Viacord, LLC’s devices?
Viacord, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) system. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers, regulators, and other stakeholders to identify and verify the devices in use.
How are Viacord, LLC’s devices classified under regulatory frameworks?
Viacord, LLC’s umbilical cord blood collection sets fall under regulatory classifications relevant to in vitro diagnostics and cellular therapy collection devices. These classifications are determined by the FDA based on the intended use and risk level of the devices, ensuring appropriate oversight and compliance requirements.
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
- 883775553
Catalogue (6)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Newborn Stemcell Collection Kit | ViaCord Triplet Kit | FDA UDI | N/A | Active |
| Newborn Stemcell Collection Kit | ViaCord SibCon Single Kit | FDA UDI | N/A | Active |
| Newborn Stemcell Collection Kit | ViaCord SibCon Triplet Kit | FDA UDI | N/A | Active |
| Newborn Stemcell Collection Kit | ViaCord SibCon Twin Kit | FDA UDI | N/A | Active |
| Newborn Stemcell Collection Kit | ViaCord Single Kit | FDA UDI | N/A | Active |
| Newborn Stemcell Collection Kit | ViaCord Twin Kit | FDA UDI | N/A | Active |
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