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Medical Shipment

FDA UDI

Class II (US FDA UDI)

by Medical Shipment, LLC

Identity

Trade Name
Medical Shipment FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
IV Start Kit w/ CHG, Transparent Dressing & Nitrile Gloves, Sterile, 1/each FDA UDI
Model / Reference
13001 FDA UDI
Description
IV Start Kit w/ CHG, Transparent Dressing & Nitrile Gloves, Sterile, 1/each FDA UDI

Identifiers

Primary DI / UDI-DI
00850056286060 FDA UDI
FDA Product Code
LRS FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General surgical procedure kit, non-medicated, single-use

Medical Shipment by Medical Shipment, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Shipment, LLC

Sources (1)

  • FDA UDI 0e95bb33-d1ec-4850-b0d7-38411aa970e9 33 fields · synced May 30, 2026