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Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Oesophageal bougie, reusable FDA UDI
Device Name
JACKSON ESOPHAGEAL DILATOR 32FR FDA UDI
Model / Reference
IPN008048 FDA UDI
Description
JACKSON ESOPHAGEAL DILATOR 32FR FDA UDI

Identifiers

Catalog Number
507832 FDA UDI
Primary DI / UDI-DI
24026704532517 FDA UDI
FDA Product Code
KCF FDA UDI
GMDN Term
Oesophageal bougie, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Yes

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 — 26.5 Inch FDA UDI

Category: Oesophageal bougie, reusable

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

Similar devices

Also classified as Oesophageal bougie, 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 6bfe998d-edc5-45c5-af1b-0759a58089f6 36 fields · synced Jun 8, 2026