Home GUDID 00666416130016 BX Series Reusable Biopsy Forceps
Primary DI 00666416130016
Brand BX Series Reusable Biopsy Forceps
Company Primed Instruments Inc
Model BX100
Catalog number BX100
Device description Biopsy forceps with oval fenestrated jaws and needle. HIBC/UPN: M453BX1000
Published 2017-10-23
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true Product Codes# Code, Name table Code Name NON Forceps, Biopsy, Non-Electric, Reprocessed
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class NON Forceps, Biopsy, Non-Electric, Reprocessed Gastroenterology, Urology 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00666416130016 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00666416130016 00666416130016 666416130016 0666416130016
GMDN Terms# Term, Definition table Term Definition Flexible endoscopic biopsy forceps, reusable A flexible, manual, non-electrosurgical instrument intended to obtain tissue specimens during endoscopic procedures (e.g., gastro-urological endoscopy, laparoscopy, bronchoscopy, laryngoscopy) for histopathological examination. It is typically a flexible metal coil with a pair of scissors-like cups with cutting edge rims, which are operated by a control handle at the proximal end of the instrument. It is introduced into the body through an artificial orifice of the body or the working channel of the endoscope. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Device Size Text, specify 0 Device Size Text, specify 0
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 254491293 Device count 1 Premarket exempt true Lot or batch true Manufacturing date on label true No natural rubber latex true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00666416112319 80000 Series Reusable General and Rigid Cleaning Brush 0503388005 0503388005 2025-06-13 00666416112395 80000 Series Reusable General and Rigid Cleaning Brush 0503388005 0503388005 2025-06-13 00666416120925 SuperDART® ONE PASS™ Validated Channel Cleaning Kit 9144 9144-25 2025-06-13 00666416121144 SuperDART® ONE PASS™ Validated Channel Cleaning Device 9253 9253-25 2025-06-13 00666416121274 SuperDART® ONE PASS™ Validated Channel Cleaning Kit 9355 9355-25 2025-06-13 00666416121298 SuperDART® ONE PASS™ Validated Channel Cleaning Device 9293 9293-25 2025-06-13 00666416121311 SuperDART® ONE PASS™ Validated Channel Cleaning Kit 9399 9399-25 2025-06-13 00666416121335 SuperDART® ONE PASS™ Validated Channel Cleaning Device 9233 9233-25 2025-06-13 00666416121359 SuperDART® ONE PASS™ Validated Channel Cleaning Kit 9333 9333-25 2025-06-13 00666416121458 9000 Series Disposable Channel Cleaning Brush 0503388004 0503388004 2025-06-13 00666416121731 9000 Series Disposable Channel Cleaning Brush 0503388004 0503388004 2025-06-13 00666416121748 9000 Series Disposable Channel Cleaning Brush 0503388002 0503388002 2025-06-13 10666416112316 80000 Series Reusable General and Rigid Cleaning Brush 0503388005 0503388005 2025-06-13 00666416110650 80000 Series Reusable General and Rigid Cleaning Brush 0503388005 0503388005 2025-06-13 00666416120918 SuperDART® ONE PASS™ Validated Channel Cleaning Kit 9144 9144-25 2025-06-13 00666416121137 SuperDART® ONE PASS™ Validated Channel Cleaning Device 9253 9253-25 2025-06-13 00666416121267 SuperDART® ONE PASS™ Validated Channel Cleaning Kit 9355 9355-25 2025-06-13 00666416121281 SuperDART® ONE PASS™ Validated Channel Cleaning Device 9293 9293-25 2025-06-13 00666416121304 SuperDART® ONE PASS™ Validated Channel Cleaning Kit 9399 9399-25 2025-06-13 00666416121328 SuperDART® ONE PASS™ Validated Channel Cleaning Device 9233 9233-25 2025-06-13
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published M453BX910N0 BX Series Multi-Sampling Reusable Biopsy Forceps Primed Instruments Inc NON 2021-02-26 10888551001496 NA STERILMED, INC. NON 2020-09-06 10888551001540 NA STERILMED, INC. NON 2020-09-06 10888551001557 NA STERILMED, INC. NON 2020-09-06 10888551001564 NA STERILMED, INC. NON 2020-09-06 10888551001571 NA STERILMED, INC. NON 2020-09-06 10888551001588 NA STERILMED, INC. NON 2020-09-06 10888551001595 NA STERILMED, INC. NON 2020-09-06 10888551001601 NA STERILMED, INC. NON 2020-09-06 10888551001618 NA STERILMED, INC. NON 2020-09-06 10888551001625 NA STERILMED, INC. NON 2020-09-06 10888551001632 NA STERILMED, INC. NON 2020-09-06 10888551001670 NA STERILMED, INC. NON 2020-09-06 10888551001687 NA STERILMED, INC. NON 2020-09-06 10888551001694 NA STERILMED, INC. NON 2020-09-06 10888551001700 NA STERILMED, INC. NON 2020-09-06 10888551001724 NA STERILMED, INC. NON 2020-09-06 10888551001731 NA STERILMED, INC. NON 2020-09-06 10888551001748 NA STERILMED, INC. NON 2020-09-06 10888551001755 NA STERILMED, INC. NON 2020-09-06 10888551001762 NA STERILMED, INC. NON 2020-09-06 10888551013420 NA STERILMED, INC. NON 2020-09-06 10888551013437 NA STERILMED, INC. NON 2020-09-06 10888551013444 NA STERILMED, INC. NON 2020-09-06 10888551013451 NA STERILMED, INC. NON 2020-09-06 10888551013468 NA STERILMED, INC. NON 2020-09-06 10888551013475 NA STERILMED, INC. NON 2020-09-06 00666416130023 BX Series Reusable Biopsy Forceps Primed Instruments Inc NON 2017-10-23 00666416130030 BX Series Reusable Biopsy Forceps Primed Instruments Inc NON 2017-10-23 00666416130047 BX Series Reusable Biopsy Forceps Primed Instruments Inc NON 2017-10-23
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