Pranaq Pte., Ltd.
SingaporeFDA applicant, unverified FDA
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Pranaq Pte., Ltd. makes
Pranaq Pte. Ltd. manufactures the TipTraQ (TTQ001), a device designed for real-time tracking and monitoring of catheter tips within the body, likely used in procedures requiring precise positioning.
The TipTraQ (TTQ001) is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
TipTraQ (TTQ001) Ref K243268
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 659132760
FDA establishments
- Pranaq Pte. Ltd. Singapore Central Singapore · SG FEI 3036722175
Frequently asked questions
How many devices does Pranaq Pte., Ltd. have in the registry?
The registry currently lists 9 devices for Pranaq Pte., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pranaq Pte., Ltd.'s devices?
Among its 9 most recently registered devices, Pranaq Pte., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (8 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Pranaq Pte., Ltd.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Pranaq Pte., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pranaq Pte., Ltd. in the registry?
The most recently registered devices listed for Pranaq Pte., Ltd. include TipTraQ TTQ01A, TipTraQ TTQ01C, TipTraQ TTQ001 and TipTraQ TTQ01B.
Which FDA establishments are linked to Pranaq Pte., Ltd.?
1 FDA establishment is linked to Pranaq Pte., Ltd. in the registry; they are listed on the company page.