FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10888277385580 · Model: 806575022R · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE
Primary DI
10888277385580
Version / Model
806575022R
Catalog Number
806575022R
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-29
Public Version
1
Public Version Date
2025-02-06
Public Version Status
New
Public Device Record Key
66cc9cf8-09fa-43ac-8f7b-91b1f75cd3a0

Device Description

8065750264 @TURBOSONICS TAPERED ABS MICR

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
NKX Needle, phacoemulsification, reprocessed

GMDN Terms

Code Name
45069 Phacoemulsification system handpiece tip, reprocessed

Identifiers

Type ID
Package 20888277385587
Primary 10888277385580

Customer Contacts