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HERizon Disposable Endoscopic Forceps - Foreign Body Grasper

FDA UDI

Class I (US FDA UDI)

by Minerva Surgical, Inc.

Identity

Trade Name
HERizon Disposable Endoscopic Forceps - Foreign Body Grasper FDA UDI
Generic Name
Rigid endoscopic biopsy forceps, single-use FDA UDI
Device Name
Disposable Endoscopic Forceps - Foreign Body Grasper FDA UDI
Model / Reference
JY-C-350-18-S FDA UDI
Description
Disposable Endoscopic Forceps - Foreign Body Grasper FDA UDI

Identifiers

Catalog Number
JY-C-350-18-S FDA UDI
Primary DI / UDI-DI
00850033976281 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Rigid endoscopic biopsy forceps, single-use

HERizon Disposable Endoscopic Forceps - Foreign Body Grasper 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a8717a47-79ae-4ef6-a72e-989a15a7ebb6 36 fields · synced Jun 8, 2026