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Micro Easypass

FDA UDI

Class I (US FDA UDI)

by Gm Dos Reis Industria E Comercio Ltda

Identity

Trade Name
MICRO EASYPASS FDA UDI
Generic Name
Suturing unit, reusable FDA UDI
Device Name
MICRO EASYPASS - LARGE CURVED MICRO SUTURE PASSER FDA UDI
Model / Reference
MICRO EASYPASS - LARGE CURVED MICRO SUTURE PASSER FDA UDI
Description
MICRO EASYPASS - LARGE CURVED MICRO SUTURE PASSER FDA UDI

Identifiers

Catalog Number
335-300 FDA UDI
Primary DI / UDI-DI
07899258657189 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Suturing unit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Category: Suturing unit, reusable

Micro Easypass by Gm Dos Reis Industria E Comercio Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing unit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 899d0316-16b5-49c1-8911-3addc79ded00 34 fields · synced Jun 1, 2026