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Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Aorta punch, single-use FDA UDI
Device Name
PUNCH MDP-36K DISPOSABLE PUNCH 3.6 MILLIMETERS FDA UDI
Model / Reference
IPN016379 FDA UDI
Description
PUNCH MDP-36K DISPOSABLE PUNCH 3.6 MILLIMETERS FDA UDI

Identifiers

Catalog Number
MDP-36K FDA UDI
Primary DI / UDI-DI
04026704410316 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Aorta punch, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI
Outer Diameter — 3.6 Millimeter FDA UDI

Category: Aorta punch, single-use

Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aorta punch, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 526f4c70-2da6-4fb5-b769-aeb54b5b97a0 36 fields · synced Jun 8, 2026