FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE INDUSTRIES, INC.

DI: 10888277555792 · Model: OR939K · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE INDUSTRIES, INC.
Primary DI
10888277555792
Version / Model
OR939K
Catalog Number
OR939K
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-31
Public Version
2
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
d2321567-cecd-4c06-8d12-e4b1ef14faea

Device Description

KIT, SOFT, 3000CC, TUBING 10' X 1/4"

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KDQ BOTTLE, COLLECTION, VACUUM

GMDN Terms

Code Name
44058 General surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Package 40888277555793
Primary 10888277555792

Customer Contacts