FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE RENEWAL

DI: 10888277368446 · Model: 5071323R · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
2
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE RENEWAL
Primary DI
10888277368446
Version / Model
5071323R
Catalog Number
5071323R
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
f7597994-543f-4dc6-9263-d049ad1c36ca

Device Description

5071-323 HALL INTREX BLADE SYS 1.19MM

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
63598 Surgical saw blade, reciprocating, reprocessed

Identifiers

Type ID
Package 20080196392053
Package 20888277368443
Primary 10888277368446

Customer Contacts