SharkCut

FDA UDI

Class I (US FDA UDI)

by Techcord co., Ltd

Identity

Trade Name: SharkCut FDA UDI
Generic Name: Arthroscopic shaver system blade, single-use FDA UDI
Device Name: Shaver Blade_OD 5.0 WL 128 Aggressive Stryker Type FDA UDI
Model / Reference: T1650 FDA UDI
Description: Shaver Blade_OD 5.0 WL 128 Aggressive Stryker Type FDA UDI

Identifiers

Catalog Number: T1650 FDA UDI
Primary DI / UDI-DI: 08800053401234 FDA UDI
FDA Product Code: GFA FDA UDI
GMDN Term: Arthroscopic shaver system blade, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 5.0 Millimeter FDA UDI
Length — 128 Millimeter FDA UDI

Category: Arthroscopic shaver system blade, single-use

SharkCut by Techcord co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Techcord co., Ltd

Sources (1)

FDA UDI 0b433f2a-20a2-4831-95fc-6ea9149dc0af 36 fields · synced Jun 1, 2026