First Device Tax Deposits Due Next January

Although medical device taxes will need to be paid quarterly, the first deposits are due soon after the tax takes effect next January, KPMG tax experts say.

Device makers and importers will have to make the first deposits on new device excise taxes by Jan. 29, 2013, despite the fact that it is technically a quarterly tax, warned two KPMG excise tax consultants during a March 5 webcast. The first quarterly tax returns will be due April 30.

“So it’s really important to have all your systems up and running as of Jan. 1, 2013,” said Deborah Karet...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Regulation

NextGen Dx Panel Expects Continued Limbo On LDT Regulation

 
• By 

A recent conference panel discussed the stagnation in diagnostics regulation, highlighting the FDA's failed regulatory efforts on lab-developed tests. Political and legislative challenges hinder other reforms, and concerns over Medicare reimbursement cuts loom for the clinical lab industry.

Medtech Must Address AI Risks Now Or Jeopardize Its Future Potential, Expert Warns

 

Urgent action is needed to address gaps in how risks from medical devices and diagnostics utilizing AI are identified, mitigated and managed. So says James Pink, renowned medtech regulatory expert in an interview with Medtech Insight.

No EUDAMED, No Market: ‘Waiting Until Mandatory Deadline Is Risky’

 

EirMed CEO Richard Houlihan warns that EUDAMED (the European database on medical devices) publication delays may harm medical device manufacturers. Currently, only a fraction of the required uploads have occurred, creating potential compliance risks as the mandatory deadline approaches.

Medical Device Recalls Down In Q1 For Lowest Quarterly Count In 3 Years. But Will It Last?

 

Despite a surge in product recalls across five key industries in the first quarter of the year, medical device recalls were down, according to Sedgwick’s latest recall index. But the firm noted they’ve since ticked up.

More from Policy & Regulation

Exercise Caution While Using Hyperbaric Oxygen Therapy Devices, FDA Warns

 

The US FDA has published a list of recommendations for the safe use of hyperbaric oxygen therapy devices. While the therapy can be effective in treating several conditions, the agency says providers need to understand its potential risks.

Germany Readies For Its EPR October Revolution

 
• By 

Germany’s electronic patient record – ePA – is a flagship initiative of the ongoing national healthcare reform. The medtech industry welcomes rollout of the ePA while calling for further improvements.

No EUDAMED, No Market: ‘Waiting Until Mandatory Deadline Is Risky’

 

EirMed CEO Richard Houlihan warns that EUDAMED (the European database on medical devices) publication delays may harm medical device manufacturers. Currently, only a fraction of the required uploads have occurred, creating potential compliance risks as the mandatory deadline approaches.