← Back to catalogue

STILLE Bone Rongeurs

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name
STILLE Bone Rongeurs FDA UDI
Generic Name
Orthopaedic joint/limb rongeur FDA UDI
Device Name
BONE RONGEUR BEYER STILLE curved 17 cm 6.75 in FDA UDI
Model / Reference
105-17030 FDA UDI
Description
BONE RONGEUR BEYER STILLE curved 17 cm 6.75 in FDA UDI

Identifiers

Catalog Number
105-17030 FDA UDI
Primary DI / UDI-DI
07332339203894 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Orthopaedic joint/limb 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Dimensions & Sizes

Size
Length — 17 Centimeter FDA UDI

Category: Orthopaedic joint/limb rongeur

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

Similar devices

Also classified as Orthopaedic joint/limb rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI 7fdfb90d-5268-48c2-8d66-fae278b8fd1d 36 fields · synced Jun 8, 2026