SEARCH RESULTS FOR: gs1(83 results)

Company Name

• Aesculap AG (83)

Brand Name

• PROSPACE® (52)
• TSPACE® PEEK (25)
• A-SPACE (6)

GMDN Term Name

• Polymeric spinal interbody fusion cage (83)

GMDN Term Status

• Active (83)

FDA Product Code Name

• Intervertebral fusion device with bone graft, lumbar (83)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (6)

FDA Product Code

• MAX (83)
• MQP (6)

Device Packaged As Sterile

• Yes (83)

Sterilization Prior To Use

• No (83)

Issuing Agency

• GS1 (83)

Device Size Type

• Length : 26.000 MM (83)
• Degree (°) : 5.000 DEG (43)
• Degree (°) : 0.000 DEG (18)
• Degree (°) : 8.000 DEG (16)
• Height : 11.000 MM (10)
• Height : 13.000 MM (10)
• Height : 15.000 MM (10)
• Height : 17.000 MM (10)
• Height : 9.000 MM (10)
• Height : 10.000 MM (8)
• Height : 12.000 MM (8)
• Height : 8.000 MM (8)
• Height : 7.000 MM (7)
• Degree (°) : 6.000 DEG (6)
• Height : 14.000 MM (1)
• Height : 19.000 MM (1)

Device Class

• Class II (83)

Implantable

• Yes (83)