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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Intrauterine cannula, reusable FDA UDI
Device Name
CANNULA COEN ACORN INTRAUTERINE PROBE FDA UDI
Model / Reference
IPN022817 FDA UDI
Description
CANNULA COEN ACORN INTRAUTERINE PROBE FDA UDI

Identifiers

Catalog Number
P42849 FDA UDI
Primary DI / UDI-DI
34026704656012 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Intrauterine cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Category: Intrauterine cannula, reusable

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

Similar devices

Also classified as Intrauterine cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI f5af1117-897f-47ef-9f6b-e4c31f94931c 35 fields · synced Jun 1, 2026