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EMI Dental Micro Needle Holder

FDA UDI

Class I (US FDA UDI)

by Emi Factory Co., Ltd.

Identity

Trade Name
EMI Dental Micro Needle Holder FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
The product is intended to be used for the purpose of grasping the suture needle during suturing. FDA UDI
Model / Reference
EMI087D 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
04582486866913 FDA UDI
FDA Product Code
FHQ FDA UDI
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Suturing needle holder, reusable

EMI Dental Micro Needle Holder by Emi Factory Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing needle holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e03a56f-af60-43ff-a633-f7de2988e510 34 fields · synced May 31, 2026