Pleatman Sac

FDA UDI

Class II (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name: PLEATMAN SAC FDA UDI
Generic Name: Tissue extraction bag FDA UDI
Device Name: PLEATMAN SAC, Reusable Introducer FDA UDI
Model / Reference: 005326-901 FDA UDI
Description: PLEATMAN SAC, Reusable Introducer FDA UDI

Identifiers

Primary DI / UDI-DI: 00821925000131 FDA UDI
510(k) Number: K923945 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

FDA UDI

Single Use

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Tissue extraction bag

Pleatman Sac by Gyrus Acmi, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K923945 also covers:

GYRUS ACMI — Gyrus Acmi, Inc.

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: Gyrus Acmi, Inc.

Sources (1)

FDA UDI fc2b0905-1fcb-4911-8619-f36031415390 34 fields · synced Jun 8, 2026