FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 20197344160225 · Model: AD222N · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
MEDLINE
Primary DI
20197344160225
Version / Model
AD222N
Catalog Number
AD222N
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2025-10-17
Public Version
1
Public Version Date
2025-10-27
Public Version Status
New
Public Device Record Key
20949092-4067-4ddc-a1f6-2e322d45f475

Device Description

ANGIO DRP 75X158IN W-FC PCHS

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
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
Unit of Use 10197344160228
Primary 20197344160225

Customer Contacts