SEARCH RESULTS FOR: gs1(86 results)

Company Name

• Aesculap AG (86)

Brand Name

• PROSPACE® (60)
• PROSPACE® XP (26)

GMDN Term Name

• Polymeric spinal interbody fusion cage (60)
• Metal-polymer composite spinal interbody fusion cage (26)

GMDN Term Status

• Active (86)

FDA Product Code Name

• Pedicle screw spinal system, adolescent idiopathic scoliosis (86)
• Intervertebral fusion device with bone graft, lumbar (86)

FDA Product Code

• MAX (86)

Device Packaged As Sterile

• Yes (86)

Sterilization Prior To Use

• No (86)

Issuing Agency

• GS1 (86)

Device Size Type

• Length : 22.000 MM (86)
• Degree (°) : 0.000 DEG (30)
• Degree (°) : 5.000 DEG (30)
• Degree (°) : 8.000 DEG (26)
• Height : 9.000 MM (15)
• Height : 10.000 MM (12)
• Height : 11.000 MM (12)
• Height : 12.000 MM (9)
• Height : 13.000 MM (9)
• Height : 8.000 MM (9)
• Height : 7.000 MM (8)
• Height : 15.000 MM (6)
• Height : 17.000 MM (6)

Device Class

• Class II (86)

Implantable

• Yes (86)