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Endo Retract II

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Endo Retract II FDA UDI
Generic Name
Self-retaining surgical retractor, single-use FDA UDI
Device Name
Articulating Fan Retractor FDA UDI
Model / Reference
176647 FDA UDI
Description
Articulating Fan Retractor FDA UDI

Identifiers

Primary DI / UDI-DI
10884523000856 FDA UDI
510(k) Number
K920068 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Self-retaining surgical retractor, 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 10 Millimeter FDA UDI

Category: Self-retaining surgical retractor, single-use

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

Similar devices

Also classified as Self-retaining surgical retractor, single-use.

Cleared under the same submission

K920068 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 a097cf1a-98a7-4f5f-a07d-da9c8e4c1c52 37 fields · synced Jun 8, 2026