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Lp7592

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref LP7592Model Vitrectomy/MVR Knife

by Surgistar Inc.

Identity

Trade Name
SURGISTAR FDA UDI
Generic Name
Scalpel, single-use FDA UDI
Model / Reference
Vitrectomy/MVR Knife EUDAMED
LP7592 EUDAMED
965572 FDA UDI

Identifiers

Catalog Number
LP7592 FDA UDI
Primary DI / UDI-DI
00878799001474 EUDAMEDFDA UDI
Basic UDI-DI
087879900MVRUP EUDAMED
FDA Product Code
EMF FDA UDI
EMDN Code
Q02010102 OPHTHALMIC MICROKNIVES, ANGLED EUDAMED
GMDN Term
Scalpel, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Lp7592 by Surgistar Inc. — 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
Surgistar Inc.
EUDAMED SRN
US-MF-000003747
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (2)

  • EUDAMED c8f2db39-5006-4be1-97b2-8bdb154df884 61 fields · synced Aug 4, 2026
  • FDA UDI 6e38d66b-ac3a-4b92-b35d-cbb7bf84e6f8 34 fields · synced May 30, 2026