FDA UDI In Commercial Distribution 🇺🇸 United States

Medline Industries, Inc.

DI: 10889942429370 · Model: PHS616026002A · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline Industries, Inc.
Primary DI
10889942429370
Version / Model
PHS616026002A
Catalog Number
PHS616026002A
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-30
Public Version
6
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
ece4516a-34d5-4ce1-bc4b-f9840385055b

Device Description

CRMS ANGIO PACK-LF

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OEQ Angiography/angioplasty kit

GMDN Terms

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

Identifiers

Type ID
Primary 10889942429370
Package 40889942429371

Customer Contacts