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DiLumen Interventional Grasper

FDA UDI

Class II (US FDA UDI)

by Lumendi Llc

Identity

Trade Name
DiLumen Interventional Grasper FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Device Name
125 cm flexible shaft grasper with elbow bending section and articulating distal tip FDA UDI
Model / Reference
IgE 125cm FDA UDI
Description
125 cm flexible shaft grasper with elbow bending section and articulating distal tip FDA UDI

Identifiers

Catalog Number
D-3010 FDA UDI
Primary DI / UDI-DI
00858836007102 FDA UDI
FDA Product Code
PTS FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Category: Flexible endoscopic tissue manipulation forceps, single-use

DiLumen Interventional Grasper by Lumendi Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lumendi Llc

Sources (1)

  • FDA UDI 87fd2438-273a-4505-88a8-35f50923bce2 34 fields · synced May 30, 2026