STILLE Bone Cutters

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name: STILLE Bone Cutters FDA UDI
Generic Name: Bone cutter FDA UDI
Device Name: BONE CUTTING FORCEPS ORIGINAL STILLE curved 19 cm 7.5 in FDA UDI
Model / Reference: 105-16811 FDA UDI
Description: BONE CUTTING FORCEPS ORIGINAL STILLE curved 19 cm 7.5 in FDA UDI

Identifiers

Catalog Number: 105-16811 FDA UDI
Primary DI / UDI-DI: 07332339203863 FDA UDI
FDA Product Code: HTZ FDA UDI
GMDN Term: Bone cutter FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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 — 19 Centimeter FDA UDI

Category: Bone cutter

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

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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 62eb1b3a-8d14-49d9-b6f9-8c243295e4ce 36 fields · synced Jun 8, 2026