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SCIg60

FDA UDI

Class II (US FDA UDI)

by EMED Technologies Corporation

Identity

Trade Name
SCIg60 FDA UDI
Generic Name
Ambulatory non-insulin infusion pump, mechanical, reusable FDA UDI
Device Name
SCIg60 Infusion Pump Carrying Case FDA UDI
Model / Reference
FP-0010032 FDA UDI
Description
SCIg60 Infusion Pump Carrying Case FDA UDI

Identifiers

Primary DI / UDI-DI
00817708023398 FDA UDI
510(k) Number
K142319 FDA UDI
K161906 FDA UDI
K173783 FDA UDI
K222087 FDA UDI
K240148 FDA UDI
FDA Product Code
PKP FDA UDI
GMDN Term
Ambulatory non-insulin infusion pump, mechanical, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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

Category: Ambulatory non-insulin infusion pump, mechanical, reusable

SCIg60 by EMED Technologies Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulatory non-insulin infusion pump, mechanical, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 42c58d71-3aca-498d-9518-7f9ea4ade3ab 35 fields · synced Jun 9, 2026