← Back to catalogue

RF Disposable Grounding Pad

FDA UDI

Class II (US FDA UDI)

by Celling Biosciences

Identity

Trade Name
RF Disposable Grounding Pad FDA UDI
Generic Name
Electrosurgical return electrode, single-use FDA UDI
Device Name
RF Disposable Grounding Pad Qty 20 FDA UDI
Model / Reference
#2130ac FDA UDI
Description
RF Disposable Grounding Pad Qty 20 FDA UDI

Identifiers

Catalog Number
#2130ac FDA UDI
Primary DI / UDI-DI
00817771029013 FDA UDI
510(k) Number
K102372 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical return electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical return electrode, single-use

RF Disposable Grounding Pad by Celling Biosciences — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical return electrode, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Celling Biosciences

Sources (1)

  • FDA UDI 9c49cf6b-7306-4f87-8dce-e189423822ea 35 fields · synced Jun 8, 2026