HERizon Disposable Endoscopic Forceps – Alligator

FDA UDI

Class I (US FDA UDI)

by Minerva Surgical, Inc.

Identity

Trade Name: HERizon Disposable Endoscopic Forceps – Alligator FDA UDI
Generic Name: Rigid endoscopic biopsy forceps, single-use FDA UDI
Device Name: Disposable Endoscopic Forceps – Alligator FDA UDI
Model / Reference: JY-CC-350-18-S FDA UDI
Description: Disposable Endoscopic Forceps – Alligator FDA UDI

Identifiers

Catalog Number: JY-CC-350-18-S FDA UDI
Primary DI / UDI-DI: 00850033976298 FDA UDI
FDA Product Code: HFB FDA UDI
GMDN Term: Rigid endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.4530 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Rigid endoscopic biopsy forceps, single-use

HERizon Disposable Endoscopic Forceps – Alligator by Minerva Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic biopsy forceps, single-use.

THD BIOPSY — THD SPA · Class I
LiNA OperaScope™ Biopsy Forceps — Lina Medical ApS · Class I
REDPINE — Guangzhou Red Pine Medical Instrument Co., Ltd. · Class I
OptiBite Disposable Biopsy Forceps — Micro-Tech (Nanjing) Co., Ltd. · Class I
EVONOS — Gyrus Acmi, Inc. · Class I
OptiBite Disposable Biopsy Forceps — Micro-Tech (Nanjing) Co., Ltd. · Class I
OptiBite Disposable Biopsy Forceps — Micro-Tech (Nanjing) Co., Ltd. · Class I
THD BIOPSY — THD SPA · Class I

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Minerva Surgical, Inc.

Sources (1)

FDA UDI 1b620a03-4c94-4845-9c4a-538feb6ee64e 36 fields · synced May 30, 2026