Is this your brand? Sign in to claim ownership.
Sign in to claim this brandCRANBERRY INTERNATIONAL SDN. BHD.
Malaysia·MY-MF-000004878
Last updated May 23, 2026
What CRANBERRY INTERNATIONAL SDN. BHD. makes
The company manufactures nitrile examination and treatment gloves, including powder-free and non-antimicrobial variants. Their portfolio includes specific product lines such as EVOLVE CT, REVOSOFT CT, Carbon Nitrile Powder Free Examination Gloves, Inspire Nitrile Powder Free Examination Gloves, and Zense Latex Powdered Examination Gloves.
These devices are classified as Class I under regulatory frameworks and are listed in the EU’s EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. The manufacturer is based in Malaysia.
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 Cranberry International Sdn. Bhd. manufacture?
Cranberry International Sdn. Bhd. specializes in nitrile examination and treatment gloves, including non-powdered and non-antimicrobial variants. Their product range includes specific lines like EVOLVE CT, REVOSOFT CT, Carbon Nitrile Powder Free Examination Gloves, Inspire Nitrile Powder Free Examination Gloves, and Zense Latex Powdered Examination Gloves. These gloves are designed for single-use medical procedures, ensuring barrier protection for both patients and healthcare workers.
Where is Cranberry International Sdn. Bhd. based?
The company is headquartered in Malaysia, which serves as its primary operational base for manufacturing and distributing its medical device products.
Which regulatory registries list Cranberry International Sdn. Bhd.'s devices?
The company’s devices are listed in the EU’s EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. These registries help track and verify the availability and compliance of medical devices across different regulatory jurisdictions.
How are Cranberry International Sdn. Bhd.'s devices classified under regulatory frameworks?
The devices manufactured by Cranberry International Sdn. Bhd. fall under Class I classification. This classification is typically assigned to low-risk medical devices, such as single-use gloves, where the risk to patients and users is minimal. Classification is determined by regulatory bodies based on factors like intended use, duration of contact, and potential health impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Malaysia
- Address
- NO. 1, JALAN SITAR 33/6, SEKSYEN 33, SHAH ALAM, SELANGOR, Malaysia
- Website
- www.cranberryglobal.com
- —
- —
- [email protected]
- Phone
- +603 51924802
- PRRC Contact
- Anrose Tan
- EUDAMED SRN
- MY-MF-000004878
- FDA FEI Number
- —
- DUNS Number
- 659313067
Catalogue (51)
Page 1 of 2Related Companies
Authorised Representatives
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.