FDA UDI In Commercial Distribution 🇺🇸 United States

CUSTOMED

DI: M2089000812 · Model: 712057470020 · CUSTOMED INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1000

Basic Information

Brand Name
CUSTOMED
Primary DI
M2089000812
Version / Model
712057470020
Catalog Number
900081
Company Name
CUSTOMED INC
Labeler DUNS
627572217
Distribution Status
In Commercial Distribution
Device Count in Pkg
1000
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
73b132ae-1b1c-4e56-8f49-0ef027da92c4

Device Description

STERILIZATION WRAPPER DISPOSABLE 20" X 20"

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FRG Wrap, Sterilization

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Primary M2089000812
Unit of Use M2089000810

Customer Contacts

Phone
787-622-5151

Premarket Submissions

Submission Number Supplement Number
K953678 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 20" X 20"