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Pilling IPN011482

by Teleflex Incorporated

Pilling IPN011482 (DP-48K) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 04026704410163), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04026704410163 UDI-DI Date15 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pilling
Generic name
Aorta punch, single-use
Model / Ref / Catalog
IPN011482, DP-48K
Primary DI / UDI-DI
04026704410163
FDA product code
DWS
GMDN term
Aorta punch, single-use
Device class
Class I
Regulation number
870.4500
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 4.8 Millimeter
Length — 8 Inch

Related devices

Category: Aorta punch, single-use

Similar devices in this category

Other devices filed under Aorta punch, single-use.

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See all devices from Teleflex Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)