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WIDE-EYE Polyptrap

FDA UDI

Class I (US FDA UDI)

by Boddingtons Plastics, Ltd.

Identity

Trade Name
WIDE-EYE Polyptrap FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
The WIDE-EYE Polyp Trap family is designed to attach to the suction port of an endoscope and capture excised material by applying suction through the biopsy channel of the endoscope. The product is used as a specimen transport container. FDA UDI
Model / Reference
APT013 FDA UDI
Description
The WIDE-EYE Polyp Trap family is designed to attach to the suction port of an endoscope and capture excised material by applying suction through the biopsy channel of the endoscope. The product is used as a specimen transport container. FDA UDI

Identifiers

Primary DI / UDI-DI
05060423410539 FDA UDI
FDA Product Code
NNI FDA UDI
GMDN Term
General specimen container IVD, no additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: General specimen container IVD, no additive/medium

WIDE-EYE Polyptrap by Boddingtons Plastics, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, no additive/medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boddingtons Plastics, Ltd.

Sources (1)

  • FDA UDI e5b3c93e-c3ab-4561-b773-1642b5ef3dfc 33 fields · synced May 30, 2026