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Atomlab 500 Dose Calibrator

FDA UDI

Class II (US FDA UDI)

by Biodex Medical Systems

Identity

Trade Name
Atomlab 500 Dose Calibrator FDA UDI
Generic Name
Radioisotope calibration system FDA UDI
Device Name
Atomlab 500 Dose Calibrator FDA UDI
Model / Reference
086-330 FDA UDI
Description
Atomlab 500 Dose Calibrator FDA UDI

Identifiers

Catalog Number
086-330 FDA UDI
Primary DI / UDI-DI
00718175003305 FDA UDI
510(k) Number
K090296 FDA UDI
FDA Product Code
KPT FDA UDI
GMDN Term
Radioisotope calibration system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1360 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radioisotope calibration system

Atomlab 500 Dose Calibrator by Biodex Medical Systems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radioisotope calibration system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 775f6033-7ef3-41b8-942b-1a1603e8ecbf 35 fields · synced May 30, 2026