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Flick-Catcher®

FDA UDI

Class I (US FDA UDI)

by Stanley Medical Designs, Incorporated

Identity

Trade Name
Flick-Catcher® FDA UDI
Generic Name
Wire cutter FDA UDI
Device Name
Flick-Catcher® Basket Pair, Tall (Contains 1 each of 00850013858064 and 00850013858071) FDA UDI
Model / Reference
SP-XTB-001 FDA UDI
Description
Flick-Catcher® Basket Pair, Tall (Contains 1 each of 00850013858064 and 00850013858071) FDA UDI

Identifiers

Catalog Number
SP-XTB-001 FDA UDI
Primary DI / UDI-DI
00850013858125 FDA UDI
FDA Product Code
FZT FDA UDI
GMDN Term
Wire cutter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

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: Wire cutter

Flick-Catcher® by Stanley Medical Designs, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire cutter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b6c555ac-9c1e-42ea-96eb-612f2c850766 35 fields · synced May 30, 2026