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PROGRESSIVE-LINE Pilot drill

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref J5074.3316

by ALTATEC GmbH

Identity

Trade Name
PROGRESSIVE-LINE Pilot drill EUDAMED
Guide Pilot drill, PL FDA UDI
Generic Name
Fixture/appliance dental drill bit, reusable FDA UDI
Device Name
PROGRESSIVE-LINE Drills EUDAMED
Guide Pilot drill, PL, d 2.0 mm, d 3.3 mm, L 16 mm FDA UDI
Model / Reference
J5074.3316 EUDAMEDFDA UDI
Description
Guide Pilot drill, PL, d 2.0 mm, d 3.3 mm, L 16 mm FDA UDI

Identifiers

Catalog Number
J5074.3316 FDA UDI
Primary DI / UDI-DI
04099797995534 EUDAMED
E219J507433161 FDA UDI
Basic UDI-DI
40997970004033000000000GR EUDAMED
Secondary DI
E219J507433161 EUDAMED
FDA Product Code
EJL FDA UDI
EMDN Code
Z12110102 DENTAL DRILLS EUDAMED
GMDN Term
Fixture/appliance dental drill bit, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.3240 FDA UDI
Market of Registration
Germany 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 16 Millimeter FDA UDI

PROGRESSIVE-LINE Pilot drill by ALTATEC GmbH — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ALTATEC GmbH
EUDAMED SRN
DE-MF-000006230

Sources (2)

  • EUDAMED bf6267fb-a865-4ed8-8483-c2e76cffbdc1 61 fields · synced Jun 18, 2026
  • FDA UDI 26c56c86-cd66-4907-9ea5-b1a37f56af29 36 fields · synced May 27, 2026