Bellesahouse201021violetstarroldflamess Site
3D artists often use descriptive filenames. Example:
bellesa_house_201021_violetstar_old_flames.png
– “Violetstar” could be a lighting setup (violet + star glow).
– “Old flames” – a fire effect with a vintage shader.
If you wish to turn this keyword into a story asset or game item, here is a fictional description: bellesahouse201021violetstarroldflamess
Entry #201021 – Bellesa’s House
Recorded by Violetstar, Keeper of Old Flames 3D artists often use descriptive filenames“On the 20th day of the 10th moon, I visited the abandoned dwelling of Bellesa, the fire‑weaver. The walls still whispered with ‘rold flames’ – a forgotten dialect of ember‑tongue that curls backward into time. Each violet star etched above the hearth pulsed once, then went cold. The old flames do not die; they wait.” Entry #201021 – Bellesa’s House Recorded by Violetstar,
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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