FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10197344118199 · Model: NON21006 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE
Primary DI
10197344118199
Version / Model
NON21006
Catalog Number
NON21006
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-04-25
Public Version
1
Public Version Date
2025-05-05
Public Version Status
New
Public Device Record Key
627dc05b-f952-4f64-9eb3-8f80f617d18d

Device Description

FIELD,STERILE,18"X26",FENESTRATION,2.75"

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PUI Drape, surgical, exempt

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Package 30197344118193
Primary 10197344118199
Package 20197344118196

Customer Contacts