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Eea

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
EEA FDA UDI
Generic Name
Colorectal sizer FDA UDI
Device Name
Reusable Sizer FDA UDI
Model / Reference
020250 FDA UDI
Description
Reusable Sizer FDA UDI

Identifiers

Primary DI / UDI-DI
10884521047471 FDA UDI
FDA Product Code
KOA FDA UDI
GMDN Term
Colorectal sizer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 31 Millimeter FDA UDI

Category: Colorectal sizer

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

Similar devices

Also classified as Colorectal sizer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 52094d3c-6706-42ef-b6c3-6047210b6b3b 35 fields · synced May 30, 2026