FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10888277378476 · Model: C5012AR · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10888277378476
Version / Model
C5012AR
Catalog Number
C5012AR
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-11
Public Version
1
Public Version Date
2022-05-19
Public Version Status
New
Public Device Record Key
27b8bb46-1630-4a16-8cbc-e78a8ed0b138

Device Description

C5012A @ACROMIOPLASTY ELTD (GREY) 6.5" X

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
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
61817 Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed

Identifiers

Type ID
Package 20888277378473
Primary 10888277378476

Customer Contacts