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WIZARD² Gamma Counter

REVVITY SINGAPORE PTE. LTD. · Model 3470-0150 · UDI-DI 00812589020535

JJJ Prescription
10
510(k) clearances
4
Adverse events
14
Recalls
5
Facilities

Description

An automated gamma counter to detect and count gamma radiation emitted by clinical samples that were prepared through the addition of a radioactive reagent.

Recalls

DateFirmReason
2015-12-08PerkinelmerThe content of the second #023 barcode ID label in the Barcode ID Label Binder is incorrect. The second barcode ID label #023 symbol incorrectly identifies as #024 when scanned. I
2015-12-08PerkinelmerThe content of the second #023 barcode ID label in the Barcode ID Label Binder is incorrect. The second barcode ID label #023 symbol incorrectly identifies as #024 when scanned. I
2015-12-08PerkinelmerThe content of the second #023 barcode ID label in the Barcode ID Label Binder is incorrect. The second barcode ID label #023 symbol incorrectly identifies as #024 when scanned. I
2015-12-08PerkinelmerThe content of the second #023 barcode ID label in the Barcode ID Label Binder is incorrect. The second barcode ID label #023 symbol incorrectly identifies as #024 when scanned. I
2015-12-08PerkinelmerThe content of the second #023 barcode ID label in the Barcode ID Label Binder is incorrect. The second barcode ID label #023 symbol incorrectly identifies as #024 when scanned. I
2015-12-08PerkinelmerThe content of the second #023 barcode ID label in the Barcode ID Label Binder is incorrect. The second barcode ID label #023 symbol incorrectly identifies as #024 when scanned. I
2015-12-08PerkinelmerThe content of the second #023 barcode ID label in the Barcode ID Label Binder is incorrect. The second barcode ID label #023 symbol incorrectly identifies as #024 when scanned. I
2015-06-03PerkinelmerError in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
2015-06-03PerkinelmerError in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
2015-06-03PerkinelmerError in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.