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Lieberman Style, Aspirating Adjustable mechanism

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref D10-5179Model D10-5000-9019

by Daud Jee Mfg. Co

Identity

Trade Name
Lieberman Style, Aspirating witth Silicon Tubing 100 CM EUDAMED
Lieberman Style, Aspirating Adjustable mechanism FDA UDI
Generic Name
Eyelid speculum, reusable FDA UDI
Device Name
Ophthalmic Speculums EUDAMED
TO EXPOSE THE OCULAR SURFACE BY PERVENTING EYELIDS FROM CLOSING FDA UDI
Model / Reference
D10-5179 EUDAMEDFDA UDI
D10-5000-9019 EUDAMED
Description
TO EXPOSE THE OCULAR SURFACE BY PERVENTING EYELIDS FROM CLOSING FDA UDI

Identifiers

Catalog Number
D10-5179 FDA UDI
Primary DI / UDI-DI
+G006D1051790D EUDAMED
G006D1051790 FDA UDI
Basic UDI-DI
++G006OphthalSpeculumU8 EUDAMED
FDA Product Code
HNC FDA UDI
EMDN Code
L1799 OPHTHALMOLOGY INSTRUMENTS, REUSABLE- OTHER EUDAMED
GMDN Term
Eyelid speculum, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.4350 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

No

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

Category: Eyelid speculum, reusable

Lieberman Style, Aspirating Adjustable mechanism by Daud Jee Mfg. Co — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Eyelid speculum, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Daud Jee Mfg. Co

Sources (2)

  • FDA UDI 6a6c3c08-68a4-492c-9b26-d6877753b96f 34 fields · synced Jun 19, 2026
  • EUDAMED fb956f84-8986-4770-a03f-aabd9548ded8 61 fields · synced Jun 19, 2026