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Forceps, Biopsy, Non-Electric, Reprocessed

Forceps, Biopsy, Non-Electric, Reprocessed is a medical device type in the Gastroenterology, Urology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.

Global Registration Data
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Forceps, Biopsy, Non-Electric, Reprocessed
Gastroenterology, Urology Medical Device Type
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Regulatory Classifications

US Regulatory Classifications

NON

View Product Code Classification

Class 1

21 CFR 876.1075

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Gastroenterology, Urology

Device Characteristics

No

No

No

Eligible

Definition

same as procode FCL except this product is for the reprocessed device. Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).

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