SEARCH RESULTS FOR: gs1(14 results)

Company Name

• BIOMET SPINE LLC (14)

Brand Name

• BAK® (6)
• LENTUR CABLE SYSTEM (4)
• Lentur™ Cable System (4)

GMDN Term Name

• Intervertebral-body internal spinal fixation system (14)

GMDN Term Status

• Active (14)

FDA Product Code Name

• Intervertebral fusion device with bone graft, lumbar (6)
• CERCLAGE, FIXATION (4)
• Cerclage, fixation (4)

FDA Product Code

• JDQ (8)
• MAX (6)

Device Packaged As Sterile

• Yes (14)

Sterilization Prior To Use

• No (14)

Issuing Agency

• GS1 (14)

Device Size Type

• 1.1MM DIA X 56CM LONG (2)
• PACKAGE ASSY (2)
• Double Cable / Crimp Pkg Assy Ti 1.1 mm ø x 56 cm Long (1)
• Interbody Implant (Ø 15 mm x 36 mm L) (1)
• Interbody Implant (Ø 17 mm x 36 mm L) (1)
• Interbody Implant (Ø 17 mm x 40 mm L) (1)
• Interbody Implant (Ø 19 mm x 36 mm L) (1)
• Interbody Implant (Ø 19 mm x 40 mm L) (1)
• Interbody Implant (Ø 21 mm x 28 mm L) (1)
• Lentur Double Cable / Crimp SS Package Assembly (1)
• Lentur Single Cable / Crimp SS Package Assembly (1)
• Single Cable / Crimp Pkg Assy Ti 1.1 mm ø x 56 cm Long (1)

Device Class

• Class II (14)

Implantable

• Yes (14)