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Shielded Decay Drum

FDA UDI

Class I (US FDA UDI)

by Biodex Medical Systems

Identity

Trade Name
SHIELDED DECAY DRUM FDA UDI
Generic Name
Radioactive waste container FDA UDI
Device Name
Drum, Decay, Shielded, .125" Lead , 30 Gallon Plastic Liner FDA UDI
Model / Reference
039-287 FDA UDI
Description
Drum, Decay, Shielded, .125" Lead , 30 Gallon Plastic Liner FDA UDI

Identifiers

Catalog Number
039-287 FDA UDI
Primary DI / UDI-DI
00718175002872 FDA UDI
FDA Product Code
KPY FDA UDI
GMDN Term
Radioactive waste container FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 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

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: Radioactive waste container

Shielded Decay Drum by Biodex Medical Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radioactive waste container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biodex Medical Systems

Sources (1)

  • FDA UDI 8f11e4f6-0ac7-4904-8890-1d8f2d6ff337 34 fields · synced May 30, 2026