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8230

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 8230Model Myringotomy/Tympanoplasty

by Surgistar Inc.

Identity

Trade Name
SURGISTAR FDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Model / Reference
Myringotomy/Tympanoplasty EUDAMED
8230 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00878799002891 EUDAMEDFDA UDI
Basic UDI-DI
087879900ENTST EUDAMED
510(k) Number
K923689 FDA UDI
FDA Product Code
GDX FDA UDI
EMDN Code
Q030301 ENT SURGERY BLADES, SINGLE-USE EUDAMED
GMDN Term
Manual scalpel blade, 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

8230 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 1e89930d-9af6-439a-9ce1-be31540af48e 61 fields · synced Jun 20, 2026
  • FDA UDI 6abaea06-d0f1-48dd-ae3f-1dc8c61e4be8 34 fields · synced May 30, 2026