FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10193489017731 · Model: ESRK3002P · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10193489017731
Version / Model
ESRK3002P
Catalog Number
ESRK3002P
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-10
Public Version
3
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
bbc088dc-c978-4216-a095-d5c393dedc1d

Device Description

PENCIL, CAUTERY, ROCKER, PTFE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
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
44681 Electrosurgical handpiece, single-use

Identifiers

Type ID
Primary 10193489017731
Package 20193489017738
Package 30193489017735

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Avoid excessive heat - protect from freezing.