← Back to catalogue

SCANLAN® Minimally-Invasive Instrumentation

FDA UDI

Class II (US FDA UDI)

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Minimally-Invasive Instrumentation FDA UDI
Generic Name
Suturing unit, reusable FDA UDI
Device Name
SCANLAN® Minimally-Invasive Knot Pusher FDA UDI
Model / Reference
9009-828-02 FDA UDI
Description
SCANLAN® Minimally-Invasive Knot Pusher FDA UDI

Identifiers

Catalog Number
9009-828-02 FDA UDI
Primary DI / UDI-DI
00846159024562 FDA UDI
510(k) Number
K945474 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Suturing unit, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suturing unit, reusable

SCANLAN® Minimally-Invasive Instrumentation by Scanlan International Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing unit, reusable.

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 f835501e-f19f-4181-a423-4304e02f9407 36 fields · synced Jun 1, 2026