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Sign in to claim this brandGREENPANDA SAFECARE INC.
US
Last updated May 23, 2026
What GREENPANDA SAFECARE INC. makes
GreenPanda SafeCare Inc. manufactures nitrile and vinyl examination and treatment gloves, both non-powdered variants. These products are designed for single-use medical procedures and patient care to reduce contamination risks.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 GreenPanda SafeCare Inc. manufacture?
GreenPanda SafeCare Inc. specializes in single-use medical gloves, specifically nitrile and vinyl examination and treatment gloves. Both variants are non-powdered, which helps minimize contamination risks during medical procedures and patient care.
Where is GreenPanda SafeCare Inc. based, and how does that affect its regulatory standing?
GreenPanda SafeCare Inc. is based in the United States. Since the company’s devices fall under FDA jurisdiction, they must comply with U.S. regulatory requirements. The FDA classifies these gloves as Class I devices, which typically require less stringent premarket review but still adhere to general controls and labeling requirements.
Are GreenPanda SafeCare Inc.’s devices listed in any regulatory registries, and why does this matter?
Yes, GreenPanda SafeCare Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This matters because the UDI system ensures traceability and transparency in the medical device supply chain, helping healthcare providers verify product authenticity, recall status, and compliance with regulatory standards.
How are GreenPanda SafeCare Inc.’s gloves classified by the FDA, and what does that classification imply?
The FDA classifies GreenPanda SafeCare Inc.’s gloves as Class I devices. This classification implies that the gloves pose minimal risk and are subject to general controls, such as good manufacturing practices (GMP) and labeling requirements. While Class I devices generally do not require premarket approval, they must still meet FDA safety and performance standards.
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
- 129509671
Catalogue (16)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Dr. Greenpanda | MPNF14 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPVF01 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPNF11 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPVF01 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPNF12 | FDA UDI | Class I | Active |
| Dr.Greenpanda | MPVF02 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPVF04 | FDA UDI | Class I | Active |
| Dr.greenpanda | MPNF14 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPNF12 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPNF13 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPVF03 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPNF11 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPVF04 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPVF02 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPNF13 | FDA UDI | Class I | Active |
| Dr. Greenpanda | MPVF03 | FDA UDI | Class I | Active |
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