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Endo Lung

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
Endo Lung FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
Clamp FDA UDI
Model / Reference
173051 FDA UDI
Description
Clamp FDA UDI

Identifiers

Primary DI / UDI-DI
10884523000788 FDA UDI
510(k) Number
K904578 FDA UDI
FDA Product Code
GET FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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 — 12 Millimeter FDA UDI

Category: Flexible endoscopic tissue manipulation forceps, reusable

Endo Lung by Covidien LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, reusable.

Cleared under the same submission

K904578 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 b5da5fb1-7604-453a-a774-e10961d3dc3a 37 fields · synced May 30, 2026