FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10888277379381 · Model: 7209650RH · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE
Primary DI
10888277379381
Version / Model
7209650RH
Catalog Number
7209650RH
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-14
Public Version
1
Public Version Date
2025-02-24
Public Version Status
New
Public Device Record Key
be3e80aa-7cd9-4aba-bb15-791e981be24b

Device Description

7209650 @ABLATOR, MONOPOLAR ABLATION PRB

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
61875 Endoscopic electrosurgical electrode, monopolar, single-use

Identifiers

Type ID
Primary 10888277379381

Customer Contacts