FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10193489082494 · Model: PAD9130F · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10193489082494
Version / Model
PAD9130F
Catalog Number
PAD9130F
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-04
Public Version
1
Public Version Date
2022-08-12
Public Version Status
New
Public Device Record Key
41586799-36f3-4a2e-97e7-13419219ca5b

Device Description

PAD, GROUNDING, UNIVERS, SOLID, UNCO

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
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
58494 Electrosurgical return electrode, single-use

Identifiers

Type ID
Package 20193489082491
Primary 10193489082494

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store product away from direct exposure to light at room temperature. It must be handled with care to avoid damage to the packaging and its content during transportation and storage.
Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius