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UKCA marking

UKCA marking

Search complete. 20 mentions across 7 episodes found for "UKCA marking".

Oct 26, 2026

Maria SkoudariHOST
22:11
So this connects directly to Chapter 8. which we covered in episode 161.
Maria SkoudariHOST
22:18
There, we talked about architects not relying solely on CE or UKCA marks, looking for independent third-party certification, and the Office for Product Safety and Standards now overseeing the construction products market.
Maria SkoudariHOST
22:35
So the CCPI accreditation gives specifiers another indicator of the quality, of the product information in front of them.
Maria SkoudariHOST
22:43
But it's worth being clear that CCPI is voluntary, so it sits alongside rather than replaces the checks we discussed in episode 161.
Maria SkoudariHOST
26:17
With the transition in approved document B to the European fire classification standards, that's your prompt to ask for the product's classification.
Maria SkoudariHOST
26:28
under BS EN 13501-1.
Maria SkoudariHOST
26:33
And as we discussed in episode 161, for third-party certification from a UCAS accredited testing and certification body, rather than relying on a CE or UKCA mark alone.
Maria SkoudariHOST
26:49
And if you're weighing up two otherwise comparable products, the fact that one manufacturer is CCPI accredited may give you more confidence in the quality and accuracy of the product safety data in front of you.
Ian SeagerHOST
20:32
Okay, in other news, Swift Fuels, those people we've spoken about before in the US who are making 100R, which is basically the replacement for lead-free fuel, effectively.
Ian SeagerHOST
20:45
They had a bunch of STCs in the States and they've got a big AML approved model list, which has now been approved by EASA and the UKCA.
Ian SeagerHOST
20:55
So there's something like 1600 extra airframes and 1200 engines spread across those that are now approved in EASA land and in the UK.
Ian SeagerHOST
21:04
That's

Unknown podcast

S3E1: Natural rubber teethers can carry traces of cancer-linked chemicals from the way they are made

Oct 19 · 4 Mentions

speaker_2HOST
2:06
It is crucial to understand that the word natural refers strictly to where the rubber came from, in the forest, not what the finished toy might release after manufacturing.
speaker_2HOST
2:14
And finally, the CE and UKCA marks you see on packaging.
speaker_2HOST
2:17
Which people often misunderstand.
speaker_2HOST
2:19
They do.

6 MINS LATER

speaker_2HOST
8:11
That is the law.
speaker_2HOST
8:12
Yes, that is the legal ceiling.
speaker_2HOST
8:14
The law sets the boundary for safety in Great Britain, and manufacturers use the CE or UKCA marks to declare compliance with that law.
speaker_2HOST
8:20
It is a firm, regulated ceiling.
Bryan ListerGUEST
30:05
You could compare it to the classification rules in the UK medical device regulation.
Bryan ListerGUEST
30:12
You could decide it's class one software and you'd be able to UKCA mark that yourselves.
Bryan ListerGUEST
30:21
But you may not necessarily be able to automatically put that product on the market in Northern Ireland because it doesn't meet the requirements of the European regulation.
Bryan ListerGUEST
30:30
So we can end up with these discrepancies, and sometimes that can make a big difference to the bottom line, the budget, because taking a product through a conformity assessment with a notified body obviously is a lot more work.

8 MINS LATER

Kate PymHOST
38:41
Because each element of the work that you have to do has an impact on the other elements.
Kate PymHOST
38:49
It will impact your marketing, whether you're a regulated medical device.
Kate PymHOST
38:53
It will impact your sales if you have to delay sales because you have to get your UKCA mark first, etc., etc.
Kate PymHOST
39:05
So there's lots of things to think about and there's lots of people that you will need to engage with or an awful lot of training courses to go on.
Monir El AzzouziHOST
6:28
And the last one, which is the most interesting one, is the powers to support the future development of a medical device licensing regime.
Monir El AzzouziHOST
6:35
So this one, I read it maybe two or three times because I was asking myself, is there not already a medical device license regime in the UK, which is the UKCA, because they are trying to go, go through that.
Monir El AzzouziHOST
6:47
Um, so yeah, and when I read it, I'm-- I think I understood it like that, but I'm not sure anymore now, that yes, the UKCA is here, but maybe we want to change it and to have something else or another pathway.
Monir El AzzouziHOST
7:01
UKCA is still valid, but this law or this amendment is mainly to be able to work on a new licensing, um, pathway regime for UK.
Monir El AzzouziHOST
7:16
So it doesn't mean that you will not accept any other way like CE marking or like, uh, maybe they will open door for reliance with the US or other things.
Monir El AzzouziHOST
7:26
But it's mainly to think of something more domestic, internal.
Monir El AzzouziHOST
7:43
It doesn't mean that they are working on it.
Monir El AzzouziHOST
7:45
It's just a wish.
JimHOST
8:06
...
JimHOST
8:06
they have got the UK, they've got UKCA approved things.
JimHOST
8:09
And maybe they're...
JimHOST
8:10
What's the, what's the, uh, is it asbestos in the bottom?
FranGUEST
8:18
God, no.
JimHOST
8:18
No, they're UK-
ScottUNKNOWN
8:19
It's UKCA, mate
JimHOST
8:19
...
James O'BrienHOST
71:04
Of course you could
NigelAUDIENCE
71:04
... is a UKCA qualification.
James O'BrienHOST
71:04
That's what a single market, that's what a single market is, isn't it?
NigelAUDIENCE
71:07
Yeah.
NigelAUDIENCE
71:08
Now, the, the, the BS 1090 is a UKCA qualification.
NigelAUDIENCE
71:14
It's, it's a, it's a different qualification.
NigelAUDIENCE
71:17
Um-

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