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Pilling IPN008208

by Teleflex Incorporated 2 variants

Pilling IPN008208 (511140) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 16 Oct 2015 (UDI-DI 24026704533637), 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 Number24026704533637 UDI-DI Date16 Oct 2015ListedStatusListed 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  • Withdrawn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
Tracheostomy tube, non-reinforced, non-customized, reusable
Model / Ref / Catalog
IPN008208, 511140
Primary DI / UDI-DI
24026704533637
FDA product code
BTO
GMDN term
Tracheostomy tube, non-reinforced, non-customized, reusable
Device class
Class II
Regulation number
868.5800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Unsafe
Size
Length — 70 Millimeter

Related devices

Category: Tracheostomy tube, non-reinforced, non-customized, reusable

Other devices from Teleflex Incorporated

  • Arrow IPNB00820 Open recall

    Class II

  • Arrow IPNB00826 Open recall

    Class II

  • Arrow IPNB00822 Open recall

    Class II

  • Arrow IPNB00827 Open recall

    Class II

See all devices from Teleflex Incorporated →

Properties

  • Sterilise before use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)