Knotilus+

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: KNOTILUS+ FDA UDI
Generic Name: Arthroscopic obturator FDA UDI
Device Name: PENCIL TIP OBTURATOR FDA UDI
Model / Reference: 3911000502 FDA UDI
Description: PENCIL TIP OBTURATOR FDA UDI

Identifiers

Catalog Number: 3911-000-502 FDA UDI
Primary DI / UDI-DI: 07613327623826 FDA UDI
FDA Product Code: NBH FDA UDI
GMDN Term: Arthroscopic obturator FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1100 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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Arthroscopic obturator

Knotilus+ by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, 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: Stryker Corp.

Sources (1)

FDA UDI 7164d155-ab10-4e54-9bb6-c26648907b3b 35 fields · synced May 29, 2026