← Back to catalogue

Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Rigid optical mediastinoscope FDA UDI
Device Name
CARLENS MEDIASTINUM SCOPE LONG FDA UDI
Model / Reference
IPN008473 FDA UDI
Description
CARLENS MEDIASTINUM SCOPE LONG FDA UDI

Identifiers

Catalog Number
522301 FDA UDI
Primary DI / UDI-DI
24026704715309 FDA UDI
510(k) Number
K990561 FDA UDI
FDA Product Code
EWY FDA UDI
GMDN Term
Rigid optical mediastinoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4720 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 162 Millimeter FDA UDI

Category: Rigid optical mediastinoscope

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

Similar devices

Also classified as Rigid optical mediastinoscope.

Cleared under the same submission

K990561 also covers:

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 5569c3c4-00ad-4e81-a6c6-990741eae405 37 fields · synced May 30, 2026