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Epix Laparoscopic Grasper

FDA UDI

Class I (US FDA UDI)

by Applied Medical Resources Corp.

Identity

Trade Name
Epix Laparoscopic Grasper FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, single-use FDA UDI
Device Name
Disposable Grasper FDA UDI
Model / Reference
C4130 FDA UDI
Description
Disposable Grasper FDA UDI

Identifiers

Primary DI / UDI-DI
00607915110147 FDA UDI
FDA Product Code
NWV FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1720 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

Dimensions & Sizes

Size
Outer Diameter — 5 Millimeter FDA UDI
Length — 35 Centimeter FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, single-use

Epix Laparoscopic Grasper by Applied Medical Resources Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI efdf2796-c576-4911-a186-c2f7b35c87ef 35 fields · synced Jun 1, 2026