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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 oesophagoscope FDA UDI
Device Name
JESBERG ESOPHAGOSCOPE 6X8X32 FDA UDI
Model / Reference
IPN008644 FDA UDI
Description
JESBERG ESOPHAGOSCOPE 6X8X32 FDA UDI

Identifiers

Catalog Number
523650P FDA UDI
Primary DI / UDI-DI
24026704205060 FDA UDI
510(k) Number
K760652 FDA UDI
FDA Product Code
EOX FDA UDI
GMDN Term
Rigid optical oesophagoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4710 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
Width — 6 Millimeter FDA UDI
Length — 320 Millimeter FDA UDI

Category: Rigid optical oesophagoscope

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

Similar devices

Also classified as Rigid optical oesophagoscope.

Cleared under the same submission

K760652 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI caf66932-db10-492a-8192-bc83051180ac 37 fields · synced Jun 8, 2026