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NOLA Dryfield System

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 300-401

by Great Lakes Dental Technologies

Identity

Trade Name
NOLA Dryfield System EUDAMED
LG DRYFIELD KIT WHITE *I FDA UDI
Generic Name
Dental cheek retractor, professional, reusable FDA UDI
Device Name
Great Lakes NOLA Dry Field System EUDAMED
LG DRYFIELD KIT WHITE *I FDA UDI
Model / Reference
300-401 EUDAMEDFDA UDI
Description
LG DRYFIELD KIT WHITE *I FDA UDI

Identifiers

Catalog Number
300-401 FDA UDI
Primary DI / UDI-DI
300-401 EUDAMED
D7753004010 FDA UDI
Basic UDI-DI
++D7753004006M EUDAMED
FDA Product Code
DYN FDA UDI
EMDN Code
Q019001 SALIVA ASPIRATORS AND SALIVA ABSORBENTS EUDAMED
GMDN Term
Dental cheek retractor, professional, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.6640 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

NOLA Dryfield System by Great Lakes Dental Technologies — Class I — 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

EUDAMED SRN
US-MF-000003408
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 4234d354-794b-46bf-a3ed-58116a71274a 61 fields · synced Jul 12, 2026
  • FDA UDI f705228f-97c0-4a0e-b916-66edd70ab00f 35 fields · synced May 24, 2026