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icotec Systems, Saw blade

FDA UDI

Class II (US FDA UDI)

by Icotec

Identity

Trade Name
icotec Systems, Saw blade FDA UDI
Generic Name
Manual surgical saw blade, rigid FDA UDI
Device Name
icotec Systems, Saw blade FDA UDI
Model / Reference
42-891 FDA UDI
Description
icotec Systems, Saw blade FDA UDI

Identifiers

Catalog Number
42-891 FDA UDI
Primary DI / UDI-DI
07640172553909 FDA UDI
FDA Product Code
NKB FDA UDI
PML FDA UDI
GMDN Term
Manual surgical saw blade, rigid FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3027 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual surgical saw blade, rigid

icotec Systems, Saw blade by Icotec — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual surgical saw blade, rigid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icotec

Sources (1)

  • FDA UDI cd911523-3983-4bae-a828-439be91b3975 35 fields · synced May 30, 2026