FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10080196415106 · Model: EICA88980RH · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE
Primary DI
10080196415106
Version / Model
EICA88980RH
Catalog Number
EICA88980RH
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
7aaf78ff-08d0-477f-9263-ca428d3923f5

Device Description

EICA8898-01 ENT COBLATOR II PROCISE MAX

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
Primary 10080196415106

Customer Contacts