← Back to catalogue

Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Surgical bulldog clamp, reusable FDA UDI
Device Name
DEBAKEY-ADSON SUCTION TUBE 8" FDA UDI
Model / Reference
IPN005368 FDA UDI
Description
DEBAKEY-ADSON SUCTION TUBE 8" FDA UDI

Identifiers

Catalog Number
351506 FDA UDI
Primary DI / UDI-DI
14026704919465 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Surgical bulldog clamp, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 8.125 Inch FDA UDI

Category: Surgical bulldog clamp, reusable

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

Similar devices

Also classified as Surgical bulldog clamp, reusable.

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

Sources (1)

  • FDA UDI dcfd0b67-57a7-4940-b335-e1ea0c136569 36 fields · synced Jun 1, 2026