FDA UDI In Commercial Distribution 🇺🇸 United States

Cervical Spine Frame

DI: 04946329317893 · Model: 08-007-22-R1 · MIZUHO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cervical Spine Frame
Primary DI
04946329317893
Version / Model
08-007-22-R1
Catalog Number
08-007-22-R1
Company Name
MIZUHO CORPORATION
Labeler DUNS
690677802
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-02
Public Version
1
Public Version Date
2021-07-12
Public Version Status
New
Public Device Record Key
a01a7023-9ee4-4904-ad17-4f3d62985248

Device Description

Cervical Spine Frame (R1)

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
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
No

Product Codes

Code Name
GDC Table, Operating-Room, Electrical

GMDN Terms

Code Name
46208 Spinal surgery positioning board

Identifiers

Type ID
Primary 04946329317893

Customer Contacts

Phone
9999999999

Device Sizes

Type Value Unit Text
Length 1200 Millimeter