FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE RENEWAL

DI: 10888277378407 · Model: 179075PR · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE RENEWAL
Primary DI
10888277378407
Version / Model
179075PR
Catalog Number
179075PR
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-09
Public Version
1
Public Version Date
2023-10-17
Public Version Status
New
Public Device Record Key
218cfa59-14bb-4225-b208-c666b1c72085

Device Description

179075P BLUNTPORT PLS, W/BLUNTGRIP ANCH

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NLM Laparoscope, general & plastic surgery, reprocessed

GMDN Terms

Code Name
61813 Laparoscopic access cannula, reprocessed

Identifiers

Type ID
Package 20888277378404
Primary 10888277378407

Customer Contacts