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Capture™

FDA UDI

Class II (US FDA UDI)

by Diversatek Healthcare

Identity

Trade Name
Capture™ FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
Four Chamber Polyp Trap FDA UDI
Model / Reference
1202-01 FDA UDI
Description
Four Chamber Polyp Trap FDA UDI

Identifiers

Catalog Number
1202-01 FDA UDI
Primary DI / UDI-DI
M7831202010 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
General specimen container IVD, no additive/medium 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: General specimen container IVD, no additive/medium

Capture™ by Diversatek Healthcare — Class II — 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
Diversatek Healthcare

Sources (1)

  • FDA UDI 387eca29-7fbf-47fd-ad54-3ed31b72f70d 35 fields · synced May 30, 2026