← Back to catalogue

Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Freestanding patient positioner, reusable FDA UDI
Device Name
LAPAROSCOPE 10MM 45 DEGREE AUTOCLAV FDA UDI
Model / Reference
IPN056771 FDA UDI
Description
LAPAROSCOPE 10MM 45 DEGREE AUTOCLAV FDA UDI

Identifiers

Catalog Number
P32423 FDA UDI
Primary DI / UDI-DI
14026704735713 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Freestanding patient positioner, 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: Freestanding patient positioner, reusable

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

Similar devices

Also classified as Freestanding patient positioner, reusable.

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 5d821204-e3c1-4565-8f7b-e7a6736814d8 35 fields · synced Jun 8, 2026