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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Rigid endoscopic stone-retrieval forceps, reusable FDA UDI
Device Name
Spoon Fcps Spring Loaded 10mm 35cm FDA UDI
Model / Reference
IPN009589 FDA UDI
Description
Spoon Fcps Spring Loaded 10mm 35cm FDA UDI

Identifiers

Catalog Number
728097 FDA UDI
Primary DI / UDI-DI
34026704649939 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Rigid endoscopic stone-retrieval forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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: Rigid endoscopic stone-retrieval forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic stone-retrieval forceps, 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 bca7ef89-fa41-47e4-b3b0-d6cc7eb8d492 35 fields · synced Jun 8, 2026