← Back to catalogue

Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Rigid optical oesophagoscope FDA UDI
Device Name
FORBES ESOPHAGEAL SPECULUM ADULT FDA UDI
Model / Reference
IPN008653 FDA UDI
Description
FORBES ESOPHAGEAL SPECULUM ADULT FDA UDI

Identifiers

Catalog Number
523677 FDA UDI
Primary DI / UDI-DI
24026704535990 FDA UDI
FDA Product Code
EPY FDA UDI
GMDN Term
Rigid optical oesophagoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.1800 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 8.75 Inch FDA UDI

Category: Rigid optical oesophagoscope

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

Similar devices

Also classified as Rigid optical oesophagoscope.

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 8f47c10a-24ff-4fcb-aeef-f7b6d6ad0485 36 fields · synced Jun 1, 2026