FDA UDI Not in Commercial Distribution 🇺🇸 United States

ZENTRUM BACK SECTION, US

DI: 00842430108693 · Model: 8000-21-U · MIZUHO ORTHOPEDIC SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ZENTRUM BACK SECTION, US
Primary DI
00842430108693
Version / Model
8000-21-U
Catalog Number
8000-21-U
Company Name
MIZUHO ORTHOPEDIC SYSTEMS, INC.
Labeler DUNS
084527241
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-27
Public Version
2
Public Version Date
2024-02-01
Public Version Status
Update
Public Device Record Key
30bf6b0d-deaf-4d64-af5f-4995e03e0784
Distribution End Date
2024-01-26

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
No

Product Codes

Code Name
GDC Table, Operating-Room, Electrical

GMDN Terms

Code Name
37255 Universal operating table top

Identifiers

Type ID
Primary 00842430108693

Customer Contacts

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
75 – 105 KiloPascal
Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
23 – 113 Degrees Fahrenheit