Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Eye muscle hook, reusable FDA UDI
Device Name: HOOK STRABISMUS VON GRAEFE SIZE 2 10 MILLIMETER TIP 14 CENTIMETER LARGE FDA UDI
Model / Reference: IPN006717 FDA UDI
Description: HOOK STRABISMUS VON GRAEFE SIZE 2 10 MILLIMETER TIP 14 CENTIMETER LARGE FDA UDI

Identifiers

Catalog Number: 422190 FDA UDI
Primary DI / UDI-DI: 24026704526011 FDA UDI
FDA Product Code: HNQ FDA UDI
GMDN Term: Eye muscle hook, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 13.5 Centimeter FDA UDI

Category: Eye muscle hook, reusable

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

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Scobee Oblique Muscle Hook, 4.5mm — AURORA SURGICAL, LLC · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI a7c75095-8bf2-4022-bdcb-8b2a661d8e2a 36 fields · synced May 30, 2026