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Sinus frontal curette

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Sinus frontal curette FDA UDI
Generic Name
Paranasal sinus curette FDA UDI
Device Name
oblong, 90° curved FDA UDI
Model / Reference
30-205-06 FDA UDI
Description
oblong, 90° curved FDA UDI

Identifiers

Catalog Number
30-205-06 FDA UDI
Primary DI / UDI-DI
04250381813225 FDA UDI
FDA Product Code
JYG FDA UDI
GMDN Term
Paranasal sinus curette 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: Paranasal sinus curette

Sinus frontal curette by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Paranasal sinus curette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spiggle & Theis Medizintechnik GmbH

Sources (1)

  • FDA UDI 234aa1ca-fa4a-4286-b2e2-109e29c6eba8 35 fields · synced Jun 8, 2026