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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Vessel approximator FDA UDI
Device Name
VAS APPROXIMATOR 15.0MM BLADES X 2MM CUPS FDA UDI
Model / Reference
IPN002333 FDA UDI
Description
VAS APPROXIMATOR 15.0MM BLADES X 2MM CUPS FDA UDI

Identifiers

Catalog Number
065181 FDA UDI
Primary DI / UDI-DI
24026704507072 FDA UDI
510(k) Number
K861924 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Vessel approximator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 0.75 Inch FDA UDI
Length — 0.75 Inch FDA UDI

Category: Vessel approximator

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

Similar devices

Also classified as Vessel approximator.

Cleared under the same submission

K861924 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI f864d1a8-80a4-4c4a-9e9d-cfcca73d49b8 37 fields · synced Jun 1, 2026