← Back to catalogue

Medical Action Industries

FDA UDI

Class II (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
Medical Action Industries FDA UDI
Generic Name
Electrosurgical tip cleaning pad FDA UDI
Device Name
Cautery: Tip Cleaner XR 300/cs FDA UDI
Model / Reference
NS8101 FDA UDI
Description
Cautery: Tip Cleaner XR 300/cs FDA UDI

Identifiers

Primary DI / UDI-DI
20809160023690 FDA UDI
510(k) Number
K030339 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical tip cleaning pad 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical tip cleaning pad

Medical Action Industries by Medical Action Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical tip cleaning pad.

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

Sources (1)

  • FDA UDI 9deab206-6423-4e43-ab32-b192a2d8a0e5 34 fields · synced May 30, 2026