← Back to catalogue

Endoplus

FDA UDI

Class II (US FDA UDI)

by Endoplus

Identity

Trade Name
Endoplus FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
5mm Strong Fenestrated Grasping Forcep, Monopolar Handle, With Rotation, 45cm FDA UDI
Model / Reference
E306MR-45 FDA UDI
Description
5mm Strong Fenestrated Grasping Forcep, Monopolar Handle, With Rotation, 45cm FDA UDI

Identifiers

Primary DI / UDI-DI
00817401022292 FDA UDI
510(k) Number
K925114 FDA UDI
FDA Product Code
HFI FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4160 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

Endoplus by Endoplus — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Cleared under the same submission

K925114 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Endoplus

Sources (1)

  • FDA UDI d51b3afe-e328-4f84-b59c-d070f9b074af 34 fields · synced May 30, 2026