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Vermed

FDA UDI

Class II (US FDA UDI)

by Graphic Controls Acquisition Corp

Identity

Trade Name
Vermed FDA UDI
Generic Name
Cytotoxic waste container FDA UDI
Device Name
SHRP18 GAL CHEMO W/PORT/DUO LID FDA UDI
Model / Reference
SHRP18 GAL CHEMO W/PORT/DUO LID FDA UDI
Description
SHRP18 GAL CHEMO W/PORT/DUO LID FDA UDI

Identifiers

Catalog Number
32028117 FDA UDI
Primary DI / UDI-DI
00009336006540 FDA UDI
510(k) Number
K071517 FDA UDI
FDA Product Code
MMK FDA UDI
GMDN Term
Cytotoxic waste container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

No

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
MRI Safety
MR Unsafe FDA UDI

Category: Cytotoxic waste container

Vermed by Graphic Controls Acquisition Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cytotoxic waste container.

Cleared under the same submission

K071517 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Graphic Controls Acquisition Corp

Sources (1)

  • FDA UDI 8f7e40de-19a1-498c-ac98-96e71ddc8ec1 36 fields · synced Jun 1, 2026