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Reliamax

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Reliamax FDA UDI
Generic Name
Open-surgery manual linear stapler, reusable FDA UDI
Device Name
Reusable Gastrointestinal Anastomosis Stapler FDA UDI
Model / Reference
GIA80RS FDA UDI
Description
Reusable Gastrointestinal Anastomosis Stapler FDA UDI

Identifiers

Primary DI / UDI-DI
10884521174887 FDA UDI
510(k) Number
K122781 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Open-surgery manual linear stapler, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 80 Millimeter FDA UDI

Category: Open-surgery manual linear stapler, reusable

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

Similar devices

Also classified as Open-surgery manual linear stapler, reusable.

Cleared under the same submission

K122781 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 0303da4d-d074-419f-9949-0fba1b05bf04 37 fields · synced Jun 1, 2026