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Skytron 22" plastic drawer

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
Skytron 22" plastic drawer FDA UDI
Generic Name
General utility supply system, ceiling-mounted FDA UDI
Device Name
DRAWER 22"W X 19.5" X 7" SINGLE 6" PLASTIC DRAWER FDA UDI
Model / Reference
H8-300-20 FDA UDI
Description
DRAWER 22"W X 19.5" X 7" SINGLE 6" PLASTIC DRAWER FDA UDI

Identifiers

Primary DI / UDI-DI
10841736114572 FDA UDI
FDA Product Code
FQO FDA UDI
GMDN Term
General utility supply system, ceiling-mounted FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General utility supply system, ceiling-mounted

Skytron 22" plastic drawer by Skytron, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General utility supply system, ceiling-mounted.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI 1005827f-8fa9-4e4f-8e5e-7a210756e845 34 fields · synced May 30, 2026