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Drills and Handpieces

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref D-SP5008-GS

by Southern Implants (Pty) Ltd

Identity

Trade Name
N/A FDA UDI
Generic Name
Fixture/appliance dental drill bit, reusable FDA UDI
Device Name
Drills and Handpieces EUDAMED
Drill Tapered GS SP1 Ø5.0x8mm FDA UDI
Model / Reference
D-SP5008-GS EUDAMEDFDA UDI
Description
Drill Tapered GS SP1 Ø5.0x8mm FDA UDI

Identifiers

Primary DI / UDI-DI
06009544046202 EUDAMEDFDA UDI
Basic UDI-DI
6009544038759C EUDAMED
Direct Marketing DI
06009544046202 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Fixture/appliance dental drill bit, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Portugal EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusable

Drills and Handpieces by Southern Implants (pty) Ltd — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
ZA-MF-000035362
Authorised Representative
Southern Implants Europe AB SE-AR-000032508

Sources (2)

  • EUDAMED 93f30eb8-8294-4bce-ad43-cd600eadcbef 61 fields · synced Jun 18, 2026
  • FDA UDI a13d9040-9a5b-4047-9404-39d0e459634a 33 fields · synced May 30, 2026