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Sign in to claim this brandADVANCED MEDICAL DESIGN CO., LTD.
US
Last updated May 30, 2026
What ADVANCED MEDICAL DESIGN CO., LTD. makes
Advanced Medical Design Co., Ltd. manufactures single-use endoscopic insufflation tubing sets designed for use during minimally invasive surgical procedures. These devices facilitate the controlled delivery of gas into the abdominal or pelvic cavity, aiding in visualization and workspace expansion during endoscopy.
The company’s products are classified as Class I medical devices under regulatory frameworks, with the tubing sets 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 Advanced Medical Design Co., Ltd. manufacture?
Advanced Medical Design Co., Ltd. specializes in single-use endoscopic insufflation tubing sets. These devices are specifically designed for use during minimally invasive surgical procedures, such as endoscopy, to deliver gas into the abdominal or pelvic cavity. This helps surgeons achieve better visualization and workspace during the procedure.
Where is Advanced Medical Design Co., Ltd. based?
Advanced Medical Design Co., Ltd. is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.
Which regulatory registries list devices manufactured by Advanced Medical Design Co., Ltd.?
Devices produced by Advanced Medical Design Co., Ltd., such as their endoscopic insufflation tubing sets, are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the United States.
How are the devices manufactured by Advanced Medical Design Co., Ltd. classified under medical device regulations?
The company’s endoscopic insufflation tubing sets fall under Class I medical device classification. This classification is typically assigned to devices posing minimal risk to patients, such as those with simple design and low-risk use, like single-use tubing sets for controlled gas delivery during endoscopy.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- amdintl.com.tw
- —
- —
- [email protected]
- Phone
- +88622902627
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 656305567
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| The O R Company - InsufflatOR Tubing Set | PFITF-10 | EUDAMEDFDA UDI | Class I | Active |
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