Endo Bag

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name: Endo Bag FDA UDI
Generic Name: Tissue extraction bag FDA UDI
Device Name: Specimen Retrieval System FDA UDI
Model / Reference: 25040 FDA UDI
Description: Specimen Retrieval System FDA UDI

Identifiers

Primary DI / UDI-DI: 10884523000979 FDA UDI
510(k) Number: K913762 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: Tissue extraction bag 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Width — 5 Inch FDA UDI
Height — 8 Inch FDA UDI

Category: Tissue extraction bag

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

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Cleared under the same submission

K913762 also covers:

Endo Bag — Covidien LP

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Covidien LP

Sources (1)

FDA UDI 60df12ed-54f4-47a0-8e1d-4bc728067ce6 36 fields · synced May 30, 2026