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Tenaculum, Double Action

FDA UDI

Class II (US FDA UDI)

by National Advanced Endoscopy Devices, Inc.

Identity

Trade Name
Tenaculum, Double Action FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
A semi-rigid forcep inserted through the working channel of an endoscope to grasp tissue or other foreign bodies. It has a leur port for cleaning. FDA UDI
Model / Reference
86422341 FDA UDI
Description
A semi-rigid forcep inserted through the working channel of an endoscope to grasp tissue or other foreign bodies. It has a leur port for cleaning. FDA UDI

Identifiers

Catalog Number
86422341 FDA UDI
Primary DI / UDI-DI
00848657075190 FDA UDI
FDA Product Code
HIH FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Flexible endoscopic tissue manipulation forceps, reusable

Tenaculum, Double Action by National Advanced Endoscopy Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
National Advanced Endoscopy Devices, Inc.

Sources (1)

  • FDA UDI c51d8ca3-5287-4451-bf75-823f0be55a56 35 fields · synced May 30, 2026