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Sign in to claim this brandARROW MEDSOURCE GROUP LIMITED
US
Last updated May 23, 2026
What ARROW MEDSOURCE GROUP LIMITED makes
Arrow MedSource Group Limited manufactures single-use personal protective equipment and medical supplies, including nitrile examination gloves, isolation gowns, scrub suits, and shoe covers. Their portfolio also covers general-purpose syringes, surgical caps, face masks, and respirators, all designed for healthcare and clinical settings.
The company’s devices are classified under FDA regulations as Class I and Class II, with products listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 Arrow MedSource Group Limited manufacture?
Arrow MedSource Group Limited specializes in single-use medical devices primarily for healthcare and clinical environments. Their portfolio includes nitrile examination gloves, isolation gowns, scrub suits, shoe covers, general-purpose syringes, surgical caps, face masks, and respirators. These products are designed to meet common protective and procedural needs in medical settings.
Where is Arrow MedSource Group Limited based?
Arrow MedSource Group Limited is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites may vary.
Which regulatory registries list Arrow MedSource Group Limited’s devices?
Arrow MedSource Group Limited’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for medical devices authorized under FDA regulations, allowing healthcare providers and regulators to identify and verify specific products.
How are Arrow MedSource Group Limited’s devices classified under FDA regulations?
Arrow MedSource Group Limited’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards or special controls due to moderate risk. The classification depends on the specific product and its intended use.
Why are some of Arrow MedSource Group Limited’s devices listed as single-use?
Arrow MedSource Group Limited’s devices are designed as single-use to ensure patient safety, hygiene, and infection control. Single-use products are intended for one-time use and disposal, reducing the risk of cross-contamination between patients and healthcare providers. This design aligns with best practices in clinical and healthcare settings.
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
- 686378503
Catalogue (60)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Amg | SCP0001 | FDA UDI | Class I | Active |
| Amg | BC0001 | FDA UDI | Class I | Active |
| Amg | ISOG0201 | FDA UDI | Class I | Active |
| Amg | 2012 | FDA UDI | Class I | Active |
| Amg | 2013 | FDA UDI | Class I | Active |
| Amg | 6011 | FDA UDI | Class II | Active |
| Amg | ALC0001M | FDA UDI | Class I | Active |
| Amg | SP001XXL | FDA UDI | Class I | Active |
| Amg | SP001S | FDA UDI | Class I | Active |
| Amg | 6003 | FDA UDI | Class II | Active |
| Amg | ST001S | FDA UDI | Class I | Active |
| Amg | ALC0001S | FDA UDI | Class I | Active |
| Amg | ST001M | FDA UDI | Class I | Active |
| Amg | LV240 | FDA UDI | Class I | Active |
| Amg | CG03 | FDA UDI | Class I | Active |
| Amg | AMF2103-L2 | FDA UDI | Class I | Unknown |
| Amg | 2012 | FDA UDI | Class I | Active |
| Amg | ST001XL | FDA UDI | Class I | Active |
| Amg | SQA20-01 | FDA UDI | Class I | Active |
| Amg | 2022 | FDA UDI | Class I | Active |
| Amg | 6001 | FDA UDI | Class II | Active |
| Amg | ALC0001XXXL | FDA UDI | Class I | Active |
| Amg | AMF2103-L3 | FDA UDI | Class I | Unknown |
| Amg | SP001XXXL | FDA UDI | Class I | Active |
| Amg | ALC0001XXL | FDA UDI | Class I | Active |
| Amg | ALC0001L | FDA UDI | Class I | Active |
| Amg | 2021 | FDA UDI | Class I | Active |
| Amg | 6002 | FDA UDI | Class II | Active |
| Amg | 6013 | FDA UDI | Class II | Active |
| Amg | 2023 | FDA UDI | Class I | Active |
| Amg | 1325 | FDA UDI | Class I | Active |
| Amg | 2014 | FDA UDI | Class I | Active |
| Amg | 2013 | FDA UDI | Class I | Active |
| Amg | BCRW001XL | FDA UDI | Class I | Active |
| Amg | SP001L | FDA UDI | Class I | Active |
| Amg | 2011 | FDA UDI | Class I | Active |
| Amg | 2025 | FDA UDI | Class I | Unknown |
| Amg | 9500-N95 | FDA UDI | Class II | Active |
| Amg | SCS001U | FDA UDI | Class I | Active |
| Amg | ALC0001XL | FDA UDI | Class I | Active |
| Amg | ST001XXXL | FDA UDI | Class I | Active |
| Amg | AMF2103-L3 | FDA UDI | Class I | Active |
| Amg | 2014 | FDA UDI | Class I | Active |
| Amg | 2015 | FDA UDI | Class I | Active |
| Amg | BCPB001XL | FDA UDI | Class I | Active |
| Amg | ISOG0001 | FDA UDI | Class I | Active |
| Amg | 2024 | FDA UDI | Class I | Active |
| Amg | 6012 | FDA UDI | Class II | Active |
| Amg | JSW-CA45SMS04 | FDA UDI | Class I | Active |
| Amg | 2023 | FDA UDI | Class I | Unknown |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Arrow Medsource Group Limited Hongkong · CN FEI 3016685880