Twist Drill

FDA UDI

Class I (US FDA UDI)

by Gebr. Brasseler GmbH & Co. KG

Identity

Trade Name: Twist Drill FDA UDI
Generic Name: Orthopaedic bur, reusable FDA UDI
Device Name: Twist drill Ø3,2 Cann. Ø1,7 AO Connection FDA UDI
Model / Reference: SC2801.098.TS FDA UDI
Description: Twist drill Ø3,2 Cann. Ø1,7 AO Connection FDA UDI

Identifiers

Catalog Number: SC2801.098. FDA UDI
Primary DI / UDI-DI: 14053613281925 FDA UDI
FDA Product Code: GFF FDA UDI
GMDN Term: Orthopaedic bur, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4820 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

Yes

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

Category: Orthopaedic bur, reusable

Twist Drill by Gebr. Brasseler GmbH & Co. KG — 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: Gebr. Brasseler GmbH & Co. KG

Sources (1)

FDA UDI 47c76d94-3f05-4294-94d0-82652502c13d 34 fields · synced Jun 8, 2026