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Home Focus Conveying & Filling, Packaging, Labeling & Storage

Securely, flexibly and efficiently

21. April 2020
in Conveying & Filling, Packaging, Labeling & Storage, Pharmaceuticals, Plant Construction, Engineering & Components, Trade Fairs
Multivac Pack life science and healthcare products securely, flexibly and efficiently

Picture: Multivac

Med­ical devices and sen­si­tive prod­ucts place the high­est demands on pack qual­i­ty and secure pack­ag­ing process­es. Since the trend in the med­ical sec­tor towards greater prod­uct indi­vid­u­al­i­sa­tion, com­plex­i­ty and vari­ety con­tin­ues unabat­ed, lead­ing increas­ing­ly to ever small­er batch sizes, Mul­ti­vac will be pre­sent­ing at Medtec Live 2020 a num­ber of flex­i­ble solu­tions for pack­ing small prod­uct series reli­ably and effi­cient­ly. Anoth­er focus at the trade fair will be iden­ti­fi­ca­tion and inspec­tion sys­tems, which make a major con­tri­bu­tion to high­er lev­els of prod­uct and patient safety.

From its tray­seal­er range Mul­ti­vac will be show­ing the semi-auto­mat­ic  T 260 tray­seal­er, which was spe­cial­ly devel­oped for the high demands of the med­ical devices indus­try. The fea­tures of this com­pact machine are its pre­cise tem­per­a­ture con­trol and dis­tri­b­u­tion, as well as its high­ly con­trolled seal­ing pres­sure, and it there­fore offers the max­i­mum lev­el of pack qual­i­ty, repro­ducibil­i­ty and process reliability.

Oth­er exhibits include the C 300 TC cham­ber machine, which enables ster­ile prod­ucts to be packed very secure­ly in pre-made pouch­es. All mod­els of the TC series are equipped with a tem­per­a­ture-con­trolled and per­ma­nent­ly heat­ed seal­ing bar, which means that the process­es can be cal­i­brat­ed and val­i­dat­ed. The user-friend­ly machine con­trol offers a wide range of soft­ware options, such as for exam­ple the read­ing of pro­duc­tion data.

Anoth­er trade fair high­light will be the pre­sen­ta­tion of an iden­ti­fi­ca­tion and inspec­tion sys­tem, which makes a sig­nif­i­cant con­tri­bu­tion to meet­ing the statu­to­ry require­ments for patient safe­ty. The UDI reg­u­la­tions (Unique Device Iden­ti­fi­ca­tion) require med­ical prod­ucts to be marked and iden­ti­fied unique­ly. The MDR (Med­ical Device Reg­u­la­tion) also rede­fines the role of the man­u­fac­tur­er or dis­trib­u­tor, who is now respon­si­ble for the integri­ty of the med­ical prod­uct up to the point of use.

The R 245 ther­mo­form­ing pack­ag­ing machine, which is capa­ble of being freely con­fig­ured, will be used to demon­strate the prod­uct mark­ing and the visu­al inspec­tion of the print image. This high­ly flex­i­ble machine mod­el can be used to secure­ly pack a wide range of batch sizes in many dif­fer­ent for­mats and pack­ag­ing mate­ri­als. It can also be equipped very eas­i­ly with oth­er sys­tem com­po­nents, such as for exam­ple auto­mat­ed han­dling modules.

All the machines to be shown at the trade fair are clean­room-com­pat­i­ble, and they meet all the statu­to­ry require­ments as well as the GMP, GAMP5 and ISO guidelines.

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