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Sickle knife

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Sickle knife FDA UDI
Generic Name
Nasal knife FDA UDI
Device Name
pointed, left curved, bayonet 27 cm FDA UDI
Model / Reference
90-202-02 FDA UDI
Description
pointed, left curved, bayonet 27 cm FDA UDI

Identifiers

Catalog Number
90-202-02 FDA UDI
Primary DI / UDI-DI
04250381856628 FDA UDI
FDA Product Code
KTG FDA UDI
GMDN Term
Nasal knife FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Nasal knife

Sickle knife by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3202e8e6-1d48-4629-a1db-55942d9b4a21 35 fields · synced May 31, 2026