← Back to catalogue

SuperClip Securement Clasp

FDA UDI

Class I (US FDA UDI)

by Semler Technologies, Inc.

Identity

Trade Name
SuperClip Securement Clasp FDA UDI
Generic Name
Surgical drape clip, single-use FDA UDI
Device Name
The SuperClip is a sterile, single-use clip that can be used to secure drapes, guidewires or catheters during a vascular access or other cannulation procedure. Ridges on the ergonomically curved handle enables secure manipulation, and elastomeric pads provide a secure grip on drapes, wires, and catheters. The Model 4600-20 is yellow in color. FDA UDI
Model / Reference
4600-20 FDA UDI
Description
The SuperClip is a sterile, single-use clip that can be used to secure drapes, guidewires or catheters during a vascular access or other cannulation procedure. Ridges on the ergonomically curved handle enables secure manipulation, and elastomeric pads provide a secure grip on drapes, wires, and catheters. The Model 4600-20 is yellow in color. FDA UDI

Identifiers

Catalog Number
140-0600-20 FDA UDI
Primary DI / UDI-DI
10815614020590 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Surgical drape clip, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical drape clip, single-use

SuperClip Securement Clasp by Semler Technologies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drape clip, single-use.

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 7120f40a-db63-4f86-b49a-35b536cabbf2 34 fields · synced May 30, 2026