BX Series Multi-Sampling Reusable Biopsy Forceps

FDA UDI

Class I (US FDA UDI)

by Primed Instruments Inc

Identity

Trade Name: BX Series Multi-Sampling Reusable Biopsy Forceps FDA UDI
Generic Name: Flexible endoscopic biopsy forceps, reusable FDA UDI
Device Name: Reusable biopsy forceps with serrated side fenestrated jaws capable of multiple sampling. HIBC/UPN: M453BX910N0 FDA UDI
Model / Reference: BX910N FDA UDI
Description: Reusable biopsy forceps with serrated side fenestrated jaws capable of multiple sampling. HIBC/UPN: M453BX910N0 FDA UDI

Identifiers

Catalog Number: BX910N FDA UDI
Primary DI / UDI-DI: M453BX910N0 FDA UDI
FDA Product Code: NON FDA UDI
GMDN Term: Flexible endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 876.1075 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Flexible endoscopic biopsy forceps, reusable

BX Series Multi-Sampling Reusable Biopsy Forceps by Primed Instruments Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Primed Instruments Inc

Sources (1)

FDA UDI 8944d601-6fe2-4d16-9b5e-99bac10d0bad 37 fields · synced May 30, 2026