FDA UDI In Commercial Distribution 🇺🇸 United States

CUSTOMED

DI: M20890031442 · Model: 712057103144 · CUSTOMED INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
150

Basic Information

Brand Name
CUSTOMED
Primary DI
M20890031442
Version / Model
712057103144
Catalog Number
9003144
Company Name
CUSTOMED INC
Labeler DUNS
627572217
Distribution Status
In Commercial Distribution
Device Count in Pkg
150
Record Status
Published
Publish Date
2023-08-10
Public Version
1
Public Version Date
2023-08-18
Public Version Status
New
Public Device Record Key
f7fbfd14-de7c-4bfc-a012-2a1edb4c01f2

Device Description

CUSTOMED UNDERPADS 23" X 36" , 15/BAG, 10BAG/CS

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
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
KME Bedding, Disposable, Medical

GMDN Terms

Code Name
61850 Absorbent underpad, non-antimicrobial, single-use

Identifiers

Type ID
Unit of Use M20890031440
Primary M20890031442

Device Sizes

Type Value Unit Text
Device Size Text, specify 23 X 36 IN