FDA UDI In Commercial Distribution 🇺🇸 United States

Expandable Lumbar Fusion Cage-Type I

DI: 06942438535768 · Model: F0301-B0032AE5F · Shanghai Reach Medical Instrument Co., Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Expandable Lumbar Fusion Cage-Type I
Primary DI
06942438535768
Version / Model
F0301-B0032AE5F
Company Name
Shanghai Reach Medical Instrument Co., Ltd
Labeler DUNS
530695344
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-04
Public Version
2
Public Version Date
2025-07-14
Public Version Status
Update
Public Device Record Key
bd4f883b-c867-4872-a3a3-1a1be34d40c0

Device Characteristics

Single Use
Yes
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 06942438535768