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EMI Super MicroNeedle Holder Compound

EUDAMEDFDA UDI

Class I (EU MDR)

Ref EMI087C-L16-RB-A-RC-0.1Model Needle Holder

by Emi Factory Co., Ltd.

Identity

Trade Name
EMI Super MicroNeedle Holder Compound EUDAMED
EMI Super Micro Needle Holder Compound FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
EMI Super Micro Needle Holder EUDAMED
The product is intended to be used for the purpose of grasping the suture needle during suturing. FDA UDI
Model / Reference
Needle Holder EUDAMED
EMI087C-L16-RB-A-RC-0.1 EUDAMED
EMI087C FDA UDI
Description
The product is intended to be used for the purpose of grasping the suture needle during suturing. FDA UDI

Identifiers

Primary DI / UDI-DI
04582486864360 EUDAMEDFDA UDI
Basic UDI-DI
458248686SMNHPN EUDAMED
Direct Marketing DI
04582486864360 EUDAMED
FDA Product Code
FHQ FDA UDI
EMDN Code
L1004 MICROSURGERY NEEDLE HOLDERS, REUSABLE EUDAMED
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
876.4730 FDA UDI
Market of Registration
Italy 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

EMI Super MicroNeedle Holder Compound by Emi Factory Co., Ltd. — 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
JP-MF-000025742
Authorised Representative
Mitaka Europe GmbH DE-AR-000006361

Sources (2)

  • EUDAMED bc3d74c7-b3e7-423e-98a6-049d08111aad 61 fields · synced Jun 19, 2026
  • FDA UDI d9be153a-85b9-460f-ac05-a0689a3ce5bf 34 fields · synced May 30, 2026