Ecco

FDA UDI

Class I (US FDA UDI)

by B. Ali Impex

Identity

Trade Name: ECCO FDA UDI
Generic Name: Tooth extraction forceps FDA UDI
Device Name: ECCO – PEDO Extraction Forceps Kit 7pcs - #PEDO KIT 1pk FDA UDI
Model / Reference: 402381 FDA UDI
Description: ECCO – PEDO Extraction Forceps Kit 7pcs - #PEDO KIT 1pk FDA UDI

Identifiers

Primary DI / UDI-DI: 08964003163754 FDA UDI
FDA Product Code: EMG FDA UDI
GMDN Term: Tooth extraction forceps FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tooth extraction forceps

Ecco by B. Ali Impex — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: B. Ali Impex

Sources (1)

FDA UDI 39b980d2-cb71-4a74-ba29-ab0bb94e7c02 33 fields · synced Jun 7, 2026