← Back to catalogue

Padlock Clip

FDA UDI

Class II (US FDA UDI)

by US Endoscopy

Identity

Trade Name
Padlock Clip FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Device Name
The Padlock Clip EFTR Kit includes the EFTR Device, Raptor grasping device, and TouchSoft Coagulator Probe. It is designed for use in a flexible endoscope intended for the diagnostic tissue acquisition and full-thickness resection through the removal of lesions in the colon and rectum. FDA UDI
Model / Reference
00713229 FDA UDI
Description
The Padlock Clip EFTR Kit includes the EFTR Device, Raptor grasping device, and TouchSoft Coagulator Probe. It is designed for use in a flexible endoscope intended for the diagnostic tissue acquisition and full-thickness resection through the removal of lesions in the colon and rectum. FDA UDI

Identifiers

Catalog Number
00713229 FDA UDI
Primary DI / UDI-DI
00724995226732 FDA UDI
510(k) Number
K240274 FDA UDI
K250842 FDA UDI
FDA Product Code
FDI FDA UDI
KNS FDA UDI
PKL FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4300 FDA UDI
876.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 230 Centimeter FDA UDI
Outer Diameter — 2.4 Millimeter FDA UDI

Category: Flexible endoscopic tissue manipulation forceps, single-useGastrointestinal endoscopic clip, long-term, non-bioabsorbableInert gas-enhanced endoscopic electrosurgical electrode, reusable

Padlock Clip by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inert gas-enhanced endoscopic electrosurgical electrode, reusable.

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
US Endoscopy

Sources (1)

  • FDA UDI 7d1fec18-53c8-45be-a529-474a76836ab3 38 fields · synced May 30, 2026