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4 Chamber Polyp Trap

FDA UDI

Class II (US FDA UDI)

by Endo-Therapeutics, Inc.

Identity

Trade Name
4 Chamber Polyp Trap FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
Suction system canister, 4 chambers, fixed FDA UDI
Model / Reference
AT-PT-4-12 FDA UDI
Description
Suction system canister, 4 chambers, fixed FDA UDI

Identifiers

Catalog Number
AT-PT-4-12 FDA UDI
Primary DI / UDI-DI
00816207021171 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Surgical suction system collection container, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical suction system collection container, single-use

4 Chamber Polyp Trap by Endo-Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endo-Therapeutics, Inc.

Sources (1)

  • FDA UDI 8119e5bc-2e51-4cfd-8eab-824a61688dbf 37 fields · synced May 30, 2026