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Frontal sinus circular punch

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Frontal sinus circular punch FDA UDI
Generic Name
Bone-coring punch, reusable FDA UDI
Device Name
60°, egg-form, 90° cutting, irrig. chan. 4.5 mm, 16 cm FDA UDI
Model / Reference
30-428-45 FDA UDI
Description
60°, egg-form, 90° cutting, irrig. chan. 4.5 mm, 16 cm FDA UDI

Identifiers

Catalog Number
30-428-45 FDA UDI
Primary DI / UDI-DI
04250381894637 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Bone-coring punch, reusable 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: Bone-coring punch, reusable

Frontal sinus circular punch by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-coring punch, reusable.

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 1e2e8b6f-6837-4505-97a5-34ad1e0c37a3 35 fields · synced May 30, 2026