← Back to catalogue

Amplatz

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Amplatz FDA UDI
Generic Name
Endoscopic-access dilator, single-use FDA UDI
Device Name
Amplatz Dilator FDA UDI
Model / Reference
G17950 FDA UDI
Description
Amplatz Dilator FDA UDI

Identifiers

Catalog Number
VTD-160030-ARI FDA UDI
Primary DI / UDI-DI
00827002179509 FDA UDI
FDA Product Code
KOE FDA UDI
GMDN Term
Endoscopic-access dilator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5520 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic-access dilator, single-use

Amplatz by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic-access dilator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 345815ba-b4d8-4300-b127-65f240d8c370 36 fields · synced Jun 8, 2026