← Back to catalogue

Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Tracheostomy tube decannulation cap FDA UDI
Device Name
DECANN STOPPER 0 1/2 CLOSURE FDA UDI
Model / Reference
IPN900863 FDA UDI
Description
DECANN STOPPER 0 1/2 CLOSURE FDA UDI

Identifiers

Catalog Number
1037810 FDA UDI
Primary DI / UDI-DI
14026704611581 FDA UDI
FDA Product Code
BTO FDA UDI
GMDN Term
Tracheostomy tube decannulation cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 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

No

FDA UDI

Lot / Batch Number

No

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

Category: Tracheostomy tube decannulation cap

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

Similar devices

Also classified as Tracheostomy tube decannulation cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI a18985a1-d3d2-45bc-bec7-dbfc431e1602 35 fields · synced May 30, 2026