Snowden-Pencer

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name: Snowden-Pencer FDA UDI
Generic Name: Rigid optical cystoscope FDA UDI
Device Name: Snowden-Pencer MIS RIGID LAPAROSCOPE, 2.9MM 300MM, 0 DEGREE FDA UDI
Model / Reference: RL3300-0 FDA UDI
Description: Snowden-Pencer MIS RIGID LAPAROSCOPE, 2.9MM 300MM, 0 DEGREE FDA UDI

Identifiers

Catalog Number: RL33000 FDA UDI
Primary DI / UDI-DI: 10885403465659 FDA UDI
FDA Product Code: FAJ FDA UDI
GMDN Term: Rigid optical cystoscope FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 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

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: Rigid optical cystoscope

Snowden-Pencer by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Rigid optical cystoscope.

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AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class II
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AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class II
AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class II

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 II	Pending data

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Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI ff504bd3-0afe-4cc9-906f-d0126cf0a0a2 35 fields · synced Jun 8, 2026