FDA UDI In Commercial Distribution 🇺🇸 United States

Velofix™ PEEK Lumbar Cage

DI: 08800015954518 · Model: PL0050 · CG MedTech Co.,Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Velofix™ PEEK Lumbar Cage
Primary DI
08800015954518
Version / Model
PL0050
Company Name
CG MedTech Co.,Ltd.
Labeler DUNS
688811082
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-31
Public Version
6
Public Version Date
2025-01-06
Public Version Status
Update
Public Device Record Key
4551bd55-38b6-4fd8-ad1d-45f80e871d18

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 08800015954518

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool dry place.