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Endo Grasp

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Endo Grasp FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Device Name
Grasper FDA UDI
Model / Reference
173030 FDA UDI
Description
Grasper FDA UDI

Identifiers

Primary DI / UDI-DI
10884523000757 FDA UDI
510(k) Number
K903205 FDA UDI
FDA Product Code
HDA FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4400 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

No

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

Category: Flexible endoscopic tissue manipulation forceps, single-use

Endo Grasp by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K903205 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 26d1900e-e277-4195-9cd9-7eb375e8d855 37 fields · synced May 30, 2026