SEARCH RESULTS FOR: gs1(24 results)

Company Name

• Aesculap AG (24)

Brand Name

• PROSPACE® (12)
• TSPACE® PEEK (8)
• A-SPACE (4)

GMDN Term Name

• Polymeric spinal interbody fusion cage (24)

GMDN Term Status

• Active (24)

FDA Product Code Name

• Intervertebral fusion device with bone graft, lumbar (24)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (4)

FDA Product Code

• MAX (24)
• MQP (4)

Device Packaged As Sterile

• Yes (24)

Sterilization Prior To Use

• No (24)

Issuing Agency

• GS1 (24)

Device Size Type

• Height : 17.000 MM (24)
• Degree (°) : 5.000 DEG (12)
• Length : 26.000 MM (10)
• Length : 22.000 MM (6)
• Degree (°) : 0.000 DEG (4)
• Degree (°) : 8.000 DEG (4)
• Length : 30.000 MM (3)
• Degree (°) : 12.000 DEG (2)
• Degree (°) : 6.000 DEG (2)
• Length : 34.000 MM (2)
• Length : 28.000 MM (1)
• Length : 31.000 MM (1)
• Length : 35.000 MM (1)

Device Class

• Class II (24)

Implantable

• Yes (24)