Vichatter-captures-forum-thread Checked May 2026
Sparkles88 (Joined: 2022-01-01, Posts: 15) Reply on: 2023-02-20, 4:30 PM
artLover23 (Joined: 2020-06-01, Posts: 100) Reply on: 2023-02-20, 12:05 PM
I came across this amazing chat interface customization feature that allows you to change the background, font styles, and even add images. Has anyone else explored this feature? What are some of your favorite customization ideas? Vichatter-captures-forum-thread Checked
Hey everyone! I just wanted to share some of my favorite Vichatter captures with you all. I've been using Vichatter for a few months now, and I'm loving the creative freedom it offers.
If you're looking for inspiration, I can share some of our favorite community-made templates. We also have a dedicated team that creates and shares new themes regularly. Hey everyone
Hi Sparkles88! Thanks for sharing your enthusiasm for Vichatter! Yes, our chat interface customization feature is quite popular among users. We've seen some amazing creations, from simple text changes to intricate designs.
Wow, those captures look amazing, Sparkles88! I've been meaning to explore more of Vichatter's features. Can you share some tips on how you achieved those glitchy effects and neon lights? If you're looking for inspiration, I can share
VicVichatterSupport (Joined: 2018-01-01, Posts: 500) Reply on: 2023-02-20, 11:10 AM
Hello
We are company of medical device type II (sterelised needle) .Level of packagings are as following:
1 ) blister (direct packaging)
2) Dispenser 30 or 100 units
3) Shelf (about 1400 dispensers)
4) Shipper same as shelf (protective carton)
1)What is the alternative at blister packaging level , if we not indicate the manufacturer details : IFU, UDI etc is allow instead ?
2) same questions on Shipper level : what is the laternative ?
In Europe,US, Canada, turkie ?
3) What are the symbol that are mandatory according with packaging level?
Dear Nathalie,
the labeling on the sterile barrier system (SBS) – I assume in your case blister level, as these maintain the sterility of your device – is regulated either by the MDR (in Europe and also Türkiye) or by the recognized consensus standard ISO 11607-1 (EU, Türkiye, USA and Canada). In any case, the regulations require the manufacturer details directly on the SBS, there is no alternative.
Or are your devices not sold individually but only in the dispensers as the point of use? Then this dispenser could be considered as the outer protective packaging of your SBS and carry all required information.
The shipping packaging is only intended for transport and thus is not considered an additional packaging level, and as such is not required to fulfill any regulatory requirements. However, in certain cases (e.g. customs) a clear indication of the manufacturer is required to make the shipment traceable.
The information required on the packaging can be found in the MDR and 21 CFR part 801 as well as ISO 11607-1, the corresponding symbols in ISO 15223-1.
Let us know if we should discuss this in more detail in a short workshop, based specifically on your own device.
Kind regards
Christopher Seib