FDA UDI In Commercial Distribution 🇺🇸 United States

HyperLight Leg Section

DI: 04946329307641 · Model: 08-075-71 · MIZUHO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HyperLight Leg Section
Primary DI
04946329307641
Version / Model
08-075-71
Catalog Number
08-075-71
Company Name
MIZUHO CORPORATION
Labeler DUNS
690677802
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-08
Public Version
1
Public Version Date
2022-04-18
Public Version Status
New
Public Device Record Key
85879a67-e618-4319-8b08-3707efc6a555

Device Description

HyperLight Leg Section

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
37255 Universal operating table top

Identifiers

Type ID
Primary 04946329307641

Customer Contacts

Phone
9999999999

Device Sizes

Type Value Unit Text
Length 565 Millimeter