FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10080196744213 · Model: DYNJP9003 · MEDLINE INDUSTRIES, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10080196744213
Version / Model
DYNJP9003
Catalog Number
DYNJP9003
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-11
Public Version
2
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
79cfe82a-515a-4a55-925a-f5e37583bdbb

Device Description

DBD-DRAPE,LITHO,ANE,STERILE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, surgical
PUI Drape, surgical, exempt

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 40080196744214
Primary 10080196744213

Customer Contacts

Device Sizes

Type Value Unit Text
Width 64 Inch
Length 110 Inch