FDA UDI In Commercial Distribution 🇺🇸 United States

Medline ReNewal

DI: 10888277378155 · Model: UMAR9602M90RH · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline ReNewal
Primary DI
10888277378155
Version / Model
UMAR9602M90RH
Catalog Number
UMAR9602M90RH
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-14
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
3fd832f0-31ed-4396-ba11-aae901aa4009

Device Description

AR-9602M-90 @OPES, ABLATOR, MENISCECTOMY

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
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
61815 Endoscopic electrosurgical handpiece/electrode, monopolar, reprocessed

Identifiers

Type ID
Primary 10888277378155

Customer Contacts

Device Sizes

Type Value Unit Text
Angle 90 degree