FDA UDI In Commercial Distribution 🇺🇸 United States

MC+

DI: 03662663021722 · Model: MC622P · LDR Spine Usa, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MC+
Primary DI
03662663021722
Version / Model
MC622P
Company Name
LDR Spine Usa, Inc.
Labeler DUNS
615789729
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
6
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
9cef0b95-0e6f-48a5-9a73-aeb607fbde26

Device Description

MC+ OPEN V.B.R.14x15.5 H6 MM

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ODP Intervertebral Fusion Device With Bone Graft, Cervical
MQP Spinal Vertebral Body Replacement Device

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 03662663021722

Customer Contacts

Phone
512-344-3333

Device Sizes

Type Value Unit Text
Width 15.5 Millimeter
Depth 14 Millimeter
Height 6 Millimeter