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Direct Drive Reposable Graspers

FDA UDI

Class I (US FDA UDI)

by Applied Medical Resources Corp.

Identity

Trade Name
Direct Drive Reposable Graspers FDA UDI
Generic Name
Rigid endoscopic grasping forceps, single-use FDA UDI
Device Name
Disposable Grasper Cartridge FDA UDI
Model / Reference
C4119 FDA UDI
Description
Disposable Grasper Cartridge FDA UDI

Identifiers

Primary DI / UDI-DI
00607915116859 FDA UDI
FDA Product Code
NWV FDA UDI
GMDN Term
Rigid endoscopic grasping 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 — 32 Centimeter FDA UDI

Category: Rigid endoscopic grasping forceps, single-use

Direct Drive Reposable Graspers by Applied Medical Resources Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic grasping forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Applied Medical Resources Corp.

Sources (1)

  • FDA UDI 7bcd440c-f564-4364-84f5-7b974323044e 35 fields · synced Jun 6, 2026