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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Vascular graft tunneller FDA UDI
Device Name
BERRY TM ANGIO ACESS TUNNELER FDA UDI
Model / Reference
IPN006026 FDA UDI
Description
BERRY TM ANGIO ACESS TUNNELER FDA UDI

Identifiers

Catalog Number
355500 FDA UDI
Primary DI / UDI-DI
24026704522976 FDA UDI
FDA Product Code
MZY FDA UDI
GMDN Term
Vascular graft tunneller FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3450 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 10.75 Inch FDA UDI

Category: Vascular graft tunneller

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

Similar devices

Also classified as Vascular graft tunneller.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI c82a0d2d-5b6b-4583-9688-e44c52fa4750 36 fields · synced Jun 8, 2026