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AMT Initial Placement Dilator Set

FDA UDI

Class II (US FDA UDI)

by Applied Medical Technology, Inc.

Identity

Trade Name
AMT Initial Placement Dilator Set FDA UDI
Generic Name
Endoscopic-access dilator, single-use FDA UDI
Device Name
AMT Initial Placement Dilator Set FDA UDI
Model / Reference
IP-DIL FDA UDI
Description
AMT Initial Placement Dilator Set FDA UDI

Identifiers

Catalog Number
IP-DIL FDA UDI
Primary DI / UDI-DI
00842071106867 FDA UDI
510(k) Number
K073034 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Endoscopic-access dilator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

Yes

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

No

FDA UDI

Category: Gastro-urological guidewire, single-useEndoscopic-access dilator, single-use

AMT Initial Placement Dilator Set by Applied Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ab234d40-9eeb-49b7-9367-c4e785e136d7 36 fields · synced Jun 9, 2026