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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
Laparoscopic blunt dissector FDA UDI
Device Name
DIAMOND-FLEX 90? ARTICULATING FORCEPS MARYLAND DISSECTOR 34CM, 5MM FDA UDI
Model / Reference
89-0510 FDA UDI
Description
DIAMOND-FLEX 90? ARTICULATING FORCEPS MARYLAND DISSECTOR 34CM, 5MM FDA UDI

Identifiers

Catalog Number
890510 FDA UDI
Primary DI / UDI-DI
10885403155581 FDA UDI
510(k) Number
K110257 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic blunt dissector 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: Laparoscopic blunt dissector

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

Similar devices

Also classified as Laparoscopic blunt dissector.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 3784315b-aafe-4a2c-9f46-2a5c54a0c43a 36 fields · synced Jun 8, 2026