FDA UDI In Commercial Distribution 🇺🇸 United States

CONVOLUTED FOAM PAD

DI: 00842430105838 · Model: 1901 · MIZUHO ORTHOPEDIC SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CONVOLUTED FOAM PAD
Primary DI
00842430105838
Version / Model
1901
Catalog Number
1901-12
Company Name
MIZUHO ORTHOPEDIC SYSTEMS, INC.
Labeler DUNS
084527241
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-21
Public Version
2
Public Version Date
2020-07-07
Public Version Status
Update
Public Device Record Key
1fdda2a0-d0c1-4070-8912-296b7dae194b

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
Yes
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
FMP Protector, Skin Pressure

GMDN Terms

Code Name
58993 General-purpose medical foam padding, single-use

Identifiers

Type ID
Package 10842430105835
Primary 00842430105838

Customer Contacts