Servet Tunг§в Ax Piеџti Te Yar ✓
: The chorus features the recurring line, "Ax piştite yar, bila dunya xirabe," which expresses a wish for the world to fall into ruin or for the apocalypse to occur because life has lost its meaning without the beloved.
: The speaker frequently invokes the "Angel of Death" (Ezraîl), asking for their life to be taken as they can no longer bear the "dark nights" spent alone. Servet Tunç Ax PiЕџti Te Yar
: Servet Tunç, a Turkish-Kurdish music producer and arranger known for blending traditional folk melodies with modern electronic elements like trap and Afro-house. : The chorus features the recurring line, "Ax
Ax Pişti Te Yar (feat. İvan Aslan) - Servet Tunç - Musixmatch Ax Pişti Te Yar (feat
: The track is often categorized under Kurdish Trap Remix or modern ethnic pop, utilizing a mid-tempo beat (approx. 94 BPM) that supports the emotional weight of the lyrics. Lyrical Themes and Translation
The title "Ax Piştî Te Yar" translates to "Oh, After You, My Darling" (or "My Love"). The lyrics focus on the devastation experienced by the speaker after a separation or loss:
is a popular Kurdish song produced and arranged by Servet Tunç , featuring vocals by İvan Aslan . The track is a poignant expression of grief and longing following the loss of a loved one, blending traditional Kurdish lyrical themes with modern electronic production. Composition and Production
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