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Lyophilized Human Dura Mater Suppliers

 EMAIL INQUIRY to  1 suppliers  
Tutogen Medical Gmbh | Address: Industriestrasse 6, Neunkirchen a Brand 91077, Germany Germany
www.tutogen.de | Send Inquiry | Phone: +49-(9134)-99 88 - 5 00
FDA Registration: 3002924436  Year Established: 1985  Annual Revenues: USD 5-10 Million  Employee Count: ~120  Quality: ISO 9001, CE Certified
Products: Bone Rasps (FDA Code: HTR), Drill Bit (FDA Code: HTW), Bone Clamp (FDA Code: HXD), Bone Fixation Screw (FDA Code: HWC), Bone Fixation Staple (FDA Code: JDR), Screwdriver (FDA Code: HXX), ...
Tutogen Medical Gmbh develops pharmaceutical and medical devices. Our allogeneic bone grafts and xenogeneic origin of orthopedic & trauma products are used successfully worldwide. Our tissue sparing T more...
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 EMAIL INQUIRY to  1 Lyophilized Human Dura Mater suppliers  
FDA Code / Regulation: LEM / 882.5975

Human dura mater is human pachymeninx tissue intended to repair defects in human dura mater.

Classification. Class II (special controls). The special control for this device is the FDA guidance document entitled "Class II Special Controls Guidance Document: Human Dura Mater." See 882.1(e) for the availability of this guidance.

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