Grippaz Corporation Limited
Thailand TH-MF-000013645 Last updated 21 Oct 2026
- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
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About
The Grippaz® fish scale pattern not only provides superior grip but serves as a reinforcing lattice that vastly improves the glove’s tensile strength and creates a rip-stop effect, making Grippaz® amongst the most robust nitrile gloves on the market. In addition to the fish scale pattern providing exceptional durability, Grippaz® extended-use gloves are made from a specially formulated nitrile compound made through molecular cross-linking that directly contributes to the overall strength of the glove.
What Grippaz Corporation Limited makes
Grippaz Corporation Limited manufactures extended-use nitrile gloves featuring a fish-scale pattern designed to enhance grip and reinforce tensile strength. The gloves incorporate a rip-stop effect to improve durability and resistance to tearing, with a molecularly cross-linked nitrile compound contributing to their structural integrity.
The company’s products fall under Class I medical devices and are registered in the EU’s eudamed database. Grippaz Corporation Limited is based in Thailand.
Frequently asked questions
What types of medical devices does Grippaz Corporation Limited manufacture?
Grippaz Corporation Limited specializes in extended-use nitrile gloves. These gloves feature a distinctive fish-scale pattern that enhances grip while reinforcing the glove’s tensile strength, creating a rip-stop effect to improve durability and resistance to tearing. The gloves are designed with a molecularly cross-linked nitrile compound to further strengthen their structure.
Where is Grippaz Corporation Limited based?
Grippaz Corporation Limited is headquartered in Thailand. The company’s location in Thailand influences its regulatory compliance and market focus, though its products are intended for global use where applicable.
In which regulatory registries are Grippaz Corporation Limited’s devices listed?
Grippaz Corporation Limited’s devices are registered in the eudamed database, which is the European Union’s central registry for medical devices. This registration is required for manufacturers to comply with EU Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR) if applicable.
How are Grippaz Corporation Limited’s devices classified under medical device regulations?
Grippaz Corporation Limited’s products fall under Class I medical device classification. This classification is typically assigned to low-risk devices, such as single-use or extended-use gloves, where the risk to patients and users is minimal. Classification is determined by factors like intended use, duration of contact with the body, and potential risks.
Information
- Country
- Thailand
- Address
- 689, Bhiraj Tower Sukhumvit Road, Bangkok, Thailand
- Website
- www.grippaz.com
- [email protected]
- Phone
- +6622613270
- PRRC contact
- John Furlong
- EUDAMED SRN
- TH-MF-000013645