FDA UDI In Commercial Distribution 🇺🇸 United States

Peridot Interbody Fusion Cage System

DI: 08800066799526 · Model: LC13-0142 · GBS Commonwealth Co.,Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Peridot Interbody Fusion Cage System
Primary DI
08800066799526
Version / Model
LC13-0142
Company Name
GBS Commonwealth Co.,Ltd.
Labeler DUNS
694609156
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-03
Public Version
1
Public Version Date
2023-11-13
Public Version Status
New
Public Device Record Key
29c3274a-9a18-40e1-b1db-78d02f69a4b3

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 08800066799526