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Snowden-Pencer

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
Snowden-Pencer FDA UDI
Generic Name
Hand-held endoscopic retractor, reusable FDA UDI
Device Name
Snowden-Pencer MIS DIAMOND-FLEX TRIANGULAR RETRACTOR, ANGLED, 60MM 5MM FDA UDI
Model / Reference
89-6111 FDA UDI
Description
Snowden-Pencer MIS DIAMOND-FLEX TRIANGULAR RETRACTOR, ANGLED, 60MM 5MM FDA UDI

Identifiers

Catalog Number
896111 FDA UDI
Primary DI / UDI-DI
10885403122828 FDA UDI
510(k) Number
K092684 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Hand-held endoscopic retractor, reusable 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Hand-held endoscopic retractor, reusable

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

Similar devices

Also classified as Hand-held endoscopic retractor, reusable.

Cleared under the same submission

K092684 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI e1fd543f-487a-44c7-ba7c-3e1bccb39e58 36 fields · synced Jun 8, 2026