Lyophilized Human Dura Mater Suppliers
EMAIL INQUIRY to 1 suppliers
Tutogen Medical Gmbh | Address: Industriestrasse 6, Neunkirchen a Brand 91077, 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), Non-Absorbable Sutures (FDA Code: GAO), Surgical Mesh (FDA Code: FTM), Non-Implanted Hemodialysis Catheters (FDA Code: MPB), Human Bone Rasps (FDA Code: HTR), Medical Rasps (FDA Code: HTR), ...
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...
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), Non-Absorbable Sutures (FDA Code: GAO), Surgical Mesh (FDA Code: FTM), Non-Implanted Hemodialysis Catheters (FDA Code: MPB), Human Bone Rasps (FDA Code: HTR), Medical Rasps (FDA Code: HTR), ...
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.
