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Sign in to claim this brandBONASSE ENTERPRISES CO., LTD.
Taiwan·TW-MF-000001352
Last updated May 30, 2026
What BONASSE ENTERPRISES CO., LTD. makes
Bonasse Enterprises Co., Ltd. manufactures contact lens cases, including reusable and disposable variants, as well as a product line called Voguestrap, which appears to include accessories or storage solutions for contact lenses. The portfolio includes multiple iterations of the BONASSE brand, likely differentiated by design or material specifications.
The company’s devices are classified under EU Class I and Class II regulations, with listings in the EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. Bonasse Enterprises Co., Ltd. is based in Taiwan.
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 Bonasse Enterprises Co., Ltd. manufacture?
Bonasse Enterprises Co., Ltd. specializes in contact lens cases, including both reusable and disposable variants. Their product line also includes a series called Voguestrap, which appears to be related to contact lens accessories or storage solutions. The company’s portfolio primarily focuses on these categories, with multiple versions of their BONASSE brand likely differentiated by design or material.
Where is Bonasse Enterprises Co., Ltd. based?
Bonasse Enterprises Co., Ltd. is headquartered in Taiwan. The company’s location is relevant for understanding regulatory compliance, as it operates under Taiwan’s medical device regulations while also listing its products in international registries like EUDAMED and the FDA’s UDI system.
Which regulatory registries list Bonasse Enterprises Co., Ltd.’s devices?
Bonasse Enterprises Co., Ltd.’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry, and the FDA’s Unique Device Identifier (UDI) system in the United States. These listings help ensure transparency and traceability of their products in global markets.
How are Bonasse Enterprises Co., Ltd.’s devices classified under medical device regulations?
Bonasse Enterprises Co., Ltd.’s devices are classified under EU medical device regulations as either Class I or Class II. Classification determines the regulatory requirements for manufacturing, labeling, and post-market surveillance. For example, Class II devices typically require additional scrutiny compared to Class I, reflecting their perceived risk level.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Taiwan
- Address
- No.11-1 Song Chiang S. Rd. Chungli District., Taoyuan City, Taiwan
- Website
- www.bonasse.com.tw
- —
- —
- [email protected]
- Phone
- +886-3-4626979
- PRRC Contact
- Elffina Lin
- EUDAMED SRN
- TW-MF-000001352
- FDA FEI Number
- —
- DUNS Number
- 657544912
Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bonasse | LT-192 | FDA UDI | Class II | Active |
| Bonasse | SC-212 | FDA UDI | Class II | Active |
| Bonasse | SC-209 | FDA UDI | Class II | Active |
| Bonasse | SC-201 | FDA UDI | Class II | Active |
| Voguestrap | SC-506 | FDA UDI | Class II | Active |
| Bonasse | SC-311 | FDA UDI | Class II | Active |
| Bonasse | BC-790+ | FDA UDI | Class II | Active |
| Bonasse | SC-110 | FDA UDI | Class II | Active |
| Voguestrap | SC-503 | FDA UDI | Class II | Active |
| Voguestrap | SC-213 | FDA UDI | Class II | Active |
| Bonasse | LC-819 | FDA UDI | Class II | Active |
| Bonasse | SC-207 | FDA UDI | Class II | Active |
| Bonasse | G-90 | FDA UDI | Class II | Active |
| Bonasse | SC-128 | FDA UDI | Class II | Active |
| Bonasse | SC-206 | FDA UDI | Class II | Active |
| Baush & Lomb | SC-160 | FDA UDI | Class II | Active |
| Bonasse | SC series | EUDAMED | Class I | Active |
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