Pt Ika Muda Corpora
IndonesiaFDA applicant, unverified
- Devices
- 1
What Pt Ika Muda Corpora makes
Pt Ika Muda Corpora manufactures latex examination gloves designed for medical and clinical use, providing a barrier for patient and user protection during examinations and procedures.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Latex Examination Gloves Ref K893275
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pt Ika Muda Corpora have in the registry?
The registry currently lists 1 device for Pt Ika Muda Corpora. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pt Ika Muda Corpora's devices?
Among its 1 most recently registered device, Pt Ika Muda Corpora has devices listed in FDA 510(k) (1 device).
What risk classes do Pt Ika Muda Corpora's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pt Ika Muda Corpora's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pt Ika Muda Corpora in the registry?
The most recently registered devices listed for Pt Ika Muda Corpora include LATEX EXAMINATION GLOVES.