FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10888277348981 · Model: 5071324R · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10888277348981
Version / Model
5071324R
Catalog Number
5071324R
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-08
Public Version
1
Public Version Date
2022-04-18
Public Version Status
New
Public Device Record Key
fe8fd390-e069-4e9c-b489-2de5141e2f33

Device Description

5071-324 INTREX SB 25.0MM X 90.0MM X 1.

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
Yes
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
GFA BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

GMDN Terms

Code Name
61803 Surgical saw blade, sagittal, reprocessed

Identifiers

Type ID
Package 10888277370326
Package 20888277348988
Primary 10888277348981

Customer Contacts