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Sign in to claim this brandAnsell
US
Last updated May 24, 2026
What Ansell makes
The company manufactures surgical gloves made from polyisoprene and polychloroprene, both in non-powdered forms. These products are designed for use in medical procedures to provide barrier protection for healthcare professionals.
The portfolio consists of Class I medical devices, which are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates with a US-based presence.
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 Ansell manufacture?
Ansell manufactures surgical gloves, specifically made from polyisoprene and polychloroprene. These gloves are designed in non-powdered forms to provide barrier protection for healthcare professionals during medical procedures. The focus is on ensuring safety and hygiene in clinical settings.
Where is Ansell based, and does it operate internationally?
Ansell has a US-based presence, meaning its headquarters or primary operations are located in the United States. While the provided data does not specify international locations, the company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, indicating regulatory engagement in the US market.
Which regulatory registries list Ansell’s devices?
Ansell’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices like their surgical gloves, ensuring transparency and traceability for regulatory and clinical purposes.
How are Ansell’s surgical gloves classified under medical device regulations?
Ansell’s surgical gloves fall under Class I medical device classification. This classification applies to devices considered low-risk, such as single-use protective barriers like gloves, which typically require less stringent regulatory oversight compared to higher-risk devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- ansell.com
- —
- —
- [email protected]
- Phone
- 775-746-6600
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 120522524
Catalogue (24)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Halyard | SGL96075 | FDA UDI | Class I | Active |
| Halyard | SGL99085 | FDA UDI | Class I | Active |
| Halyard | SGL99065 | FDA UDI | Class I | Active |
| Halyard | SGL85070B | FDA UDI | Class I | Active |
| Halyard | SGL99060 | FDA UDI | Class I | Active |
| Halyard | SGL85075B | FDA UDI | Class I | Active |
| Halyard | SGL85085B | FDA UDI | Class I | Active |
| Halyard | SGL99090 | FDA UDI | Class I | Active |
| Halyard | SGL85090B | FDA UDI | Class I | Active |
| Halyard | SGL99080 | FDA UDI | Class I | Active |
| Halyard | SGL96085 | FDA UDI | Class I | Active |
| Halyard | SGL99055 | FDA UDI | Class I | Active |
| Halyard | SGL85080B | FDA UDI | Class I | Active |
| Halyard | SGL99075 | FDA UDI | Class I | Active |
| Halyard | SGL96080 | FDA UDI | Class I | Active |
| Halyard | SGL96090 | FDA UDI | Class I | Active |
| Halyard | SGL85055B | FDA UDI | Class I | Active |
| Halyard | SGL85060B | FDA UDI | Class I | Active |
| Halyard | SGL85065B | FDA UDI | Class I | Active |
| Halyard | SGL99070 | FDA UDI | Class I | Active |
| Halyard | SGL96070 | FDA UDI | Class I | Active |
| Halyard | SGL96060 | FDA UDI | Class I | Active |
| Halyard | SGL96065 | FDA UDI | Class I | Active |
| Halyard | SGL96055 | FDA UDI | Class I | Active |
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