← Back to catalogue

Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Nasal knife FDA UDI
Device Name
BALLENGER KNIFE STRAIGHT 4 MILLIMETER FDA UDI
Model / Reference
IPN002116 FDA UDI
Description
BALLENGER KNIFE STRAIGHT 4 MILLIMETER FDA UDI

Identifiers

Catalog Number
036111 FDA UDI
Primary DI / UDI-DI
24026704505771 FDA UDI
FDA Product Code
KAS FDA UDI
GMDN Term
Nasal knife 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 19 Centimeter FDA UDI

Category: Nasal knife

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

Similar devices

Also classified as Nasal knife.

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 072ad415-f89e-4570-8c72-e5562e53e627 36 fields · synced Jun 1, 2026