← Back to catalogue

Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
Pilling FDA UDI
Generic Name
Abdominal retractor, hand-held FDA UDI
Device Name
HOLDING PIN (1) 2", EACH FDA UDI
Model / Reference
IPN002458 FDA UDI
Description
HOLDING PIN (1) 2", EACH FDA UDI

Identifiers

Catalog Number
087341 FDA UDI
Primary DI / UDI-DI
24026704598506 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Abdominal retractor, hand-held FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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 — 2 Inch FDA UDI

Category: Abdominal retractor, hand-held

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

Similar devices

Also classified as Abdominal retractor, hand-held.

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 fbaf27a4-62be-4bd0-89b4-00de049e8e7f 36 fields · synced May 30, 2026