DEVICE: Medline (10193489082494)

Device Identifier (DI) Information

Medline
PAD9130F
In Commercial Distribution
PAD9130F
MEDLINE INDUSTRIES, INC.
10193489082494
GS1

1
025460908 *Terms of Use
PAD, GROUNDING, UNIVERS, SOLID, UNCO
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Device Characteristics

Labeling does not contain MRI Safety Information
No
Yes
Yes
Yes
No
No
No
No

GMDN

[?]

GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
58494 Electrosurgical return electrode, single-use
A dispersive conductor intended to be fastened to a patient and connected to an electrosurgical/radio-frequency ablation system generator, to allow return of electrical current from the patient to the generator during an electrosurgical procedure. It has a large surface area and is fastened to the patient's body typically where the greatest surface area can be covered in closest proximity to the surgical site. It will typically be designed with permanently attached leads. This is a single-use device.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
GEI Electrosurgical, cutting & coagulation & accessories
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
Premarket Submission Number Not Available/Not Released
No CLOSE

Sterilization

No
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
Storage Environment Temperature: between 20 and 25 Degrees Celsius
Special Storage Condition, Specify: Handle with Care
Special Storage Condition, Specify: 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.
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Record Status

41586799-36f3-4a2e-97e7-13419219ca5b
October 28, 2024
2
August 04, 2022
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
20193489082491 200 10193489082494 In Commercial Distribution CASE
30193489082498 5 20193489082491 In Commercial Distribution BAG
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
No
No CLOSE

Customer Contact

[?]
+1(800)633-5463
service@medline.com
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