熱門詞： 進(jìn)口電動溫度調(diào)節(jié)閥結(jié)構(gòu)圖|進(jìn)口電動溫度調(diào)節(jié)閥數(shù)據(jù)表進(jìn)口電動高溫調(diào)節(jié)閥-德國進(jìn)口電動高溫法蘭調(diào)節(jié)閥進(jìn)口電動蒸汽調(diào)節(jié)閥-德國進(jìn)口電動蒸汽調(diào)節(jié)閥
熱門詞： 進(jìn)口電動溫度調(diào)節(jié)閥結(jié)構(gòu)圖|進(jìn)口電動溫度調(diào)節(jié)閥數(shù)據(jù)表進(jìn)口電動高溫調(diào)節(jié)閥-德國進(jìn)口電動高溫法蘭調(diào)節(jié)閥進(jìn)口電動蒸汽調(diào)節(jié)閥-德國進(jìn)口電動蒸汽調(diào)節(jié)閥
Reproline 德國Reproline
德國Reproline雙腔卵泡穿刺系統(tǒng)
The Reproline medical GmbH, situated in Rheinbach in the near of Bonn and Cologne, is specialized in the development and production of disposable products for the IVF-market like follicle puncture systems and microglass pipettes and capillaries of highest quality and technical standard. Besides that Reproline also supports IVF-centers with any kind of disposables and laboratory equipment of other brands up to fitting out complete labs.
Our own products are manufactured under clean room conditions that meet all requirements of the current US Standard categorized under Clean Room Class l0 000 according to the regulations of US FED STD 209E. Within the clean rooms you'll find facilities which correspond to Clean Room Class l00 according to US FED STD 209E.
Production and administration of Reproline medical GmbH are certified according to DIN EN ISO 9001 and DIN EN 46001.
In Germany Reproline distributes directly to the user. Abroad Reproline is represented by serious partners that are well experienced in the IVF-market.
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