STILLE Rongeurs

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name: STILLE Rongeurs FDA UDI
Generic Name: Spinal rongeur FDA UDI
Device Name: KERRISON STILLE PUNCH 20 cm 4 mm 130° up, with ejector, rubber handle, thin footplate FDA UDI
Model / Reference: 105-17643-4 FDA UDI
Description: KERRISON STILLE PUNCH 20 cm 4 mm 130° up, with ejector, rubber handle, thin footplate FDA UDI

Identifiers

Catalog Number: 105-17643-4 FDA UDI
Primary DI / UDI-DI: 07332339212742 FDA UDI
FDA Product Code: HTX FDA UDI
GMDN Term: Spinal rongeur FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 20 Centimeter FDA UDI

Category: Spinal rongeur

STILLE Rongeurs by Stille AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal rongeur.

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Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
V. Mueller — STERIS CORPORATION · Class II
Boss Instruments — Boss Instruments, Ltd. · Class II

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: Stille AB

Sources (1)

FDA UDI 6afbd6cf-7f33-46a6-8de8-16e63b4d044e 36 fields · synced Jun 8, 2026