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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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No Description
ZIRKONZAHN SRL
ZRAB1733
In Commercial Distribution

  • D800ZRAB1733 ()


  • Dental bridge, ceramic
No Description
ZIRKONZAHN SRL
ZRAB1556
In Commercial Distribution

  • D800ZRAB1556 ()


  • Dental bridge, ceramic
No Description
ZIRKONZAHN SRL
ZRAB1536
In Commercial Distribution

  • D800ZRAB1536 ()


  • Dental bridge, ceramic
No Description
ZIRKONZAHN SRL
ZRAB1442
In Commercial Distribution

  • D800ZRAB1442 ()


  • Dental bridge, ceramic
No Description
ZIRKONZAHN SRL
ZRAB1343
In Commercial Distribution

  • D800ZRAB1343 ()


  • Dental bridge, ceramic
No Description
ZIRKONZAHN SRL
ZRAB1323
In Commercial Distribution

  • D800ZRAB1323 ()


  • Dental bridge, ceramic
No Description
ZIRKONZAHN SRL
ZRAB1256
In Commercial Distribution

  • D800ZRAB1256 ()


  • Dental bridge, ceramic
Device Name: CERASORB® M DENTAL lndications for Use: CERASORB® M DENTAL is recommended for: - Augmentation or reconstructive treatment of the alveolar ridge - Filling of infrabony periodontal defects - Filling of defects after root resection, apicoectomy and cystectomy - Filling of extraction sockets to enhance preservation of the alveolar ridge - Elevation of the maxillary sinus floor - Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR) - Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
curasan AG
1000-2000µm
In Commercial Distribution

  • ECURS20M1000 ()
  • ECURS20M10005 ()

  • Total Volume: 2.0 Centiliter
5 x 2.0 cc

  • Dental bone matrix implant, synthetic
Device Name: CERASORB® M DENTAL lndications for Use: CERASORB® M DENTAL is recommended for: - Augmentation or reconstructive treatment of the alveolar ridge - Filling of infrabony periodontal defects - Filling of defects after root resection, apicoectomy and cystectomy - Filling of extraction sockets to enhance preservation of the alveolar ridge - Elevation of the maxillary sinus floor - Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR) - Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
curasan AG
500-1000µm
In Commercial Distribution

  • ECURS20M0500 ()
  • ECUS20M05005 ()

  • Total Volume: 2.0 Centiliter
5 x 2.0 cc

  • Dental bone matrix implant, synthetic
Device Name: CERASORB® M DENTAL lndications for Use: CERASORB® M DENTAL is recommended for: - Augmentation or reconstructive treatment of the alveolar ridge - Filling of infrabony periodontal defects - Filling of defects after root resection, apicoectomy and cystectomy - Filling of extraction sockets to enhance preservation of the alveolar ridge - Elevation of the maxillary sinus floor - Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR) - Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
curasan AG
150-500µm
In Commercial Distribution

  • ECURS20M0150 ()
  • ECURS20M01505 ()

  • Total Volume: 2.0 Centiliter
5 x 2.0 cc

  • Dental bone matrix implant, synthetic
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