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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Rigid optical bronchoscope FDA UDI
Device Name
HOLINGER BRONCHOSCOPE 5X40 FDA UDI
Model / Reference
IPN008491 FDA UDI
Description
HOLINGER BRONCHOSCOPE 5X40 FDA UDI

Identifiers

Catalog Number
522581 FDA UDI
Primary DI / UDI-DI
24026704715446 FDA UDI
510(k) Number
K861921 FDA UDI
FDA Product Code
LLO FDA UDI
GMDN Term
Rigid optical bronchoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4500 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

Dimensions & Sizes

Size
Length — 400 Millimeter FDA UDI

Category: Rigid optical bronchoscope

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

Similar devices

Also classified as Rigid optical bronchoscope.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6550fb90-5e41-4a99-9f79-70f576fb2743 37 fields · synced Jun 1, 2026