FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 20197344159069 · Model: MDT12091XXL · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
MEDLINE
Primary DI
20197344159069
Version / Model
MDT12091XXL
Catalog Number
MDT12091XXL
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2026-03-03
Public Version
1
Public Version Date
2026-03-11
Public Version Status
New
Public Device Record Key
ad2d31b7-629c-4f11-99f9-38a17f0d89cd

Device Description

GOWN,PROCEDURE,BLOCKADE,1PLY,CEIL,2XL

Device Characteristics

Single Use
No
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OEA Non-surgical gown

GMDN Terms

Code Name
35452 Isolation gown, reusable

Identifiers

Type ID
Unit of Use 10197344159062
Primary 20197344159069

Customer Contacts