SEARCH RESULTS FOR: gs1(60 results)

Company Name

• Aesculap AG (60)

Brand Name

• PROSPACE® (60)

GMDN Term Name

• Polymeric spinal interbody fusion cage (60)

GMDN Term Status

• Active (60)

FDA Product Code Name

• Intervertebral fusion device with bone graft, lumbar (60)

FDA Product Code

• MAX (60)

Device Packaged As Sterile

• Yes (60)

Sterilization Prior To Use

• No (60)

Issuing Agency

• GS1 (60)

Device Size Type

• Length : 22.000 MM (60)
• Degree (°) : 0.000 DEG (21)
• Degree (°) : 5.000 DEG (21)
• Degree (°) : 8.000 DEG (18)
• Height : 9.000 MM (12)
• Height : 10.000 MM (6)
• Height : 11.000 MM (6)
• Height : 12.000 MM (6)
• Height : 13.000 MM (6)
• Height : 15.000 MM (6)
• Height : 17.000 MM (6)
• Height : 7.000 MM (6)
• Height : 8.000 MM (6)

Device Class

• Class II (60)

Implantable

• Yes (60)