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Invenio

FDA UDI

Class II (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
Invenio FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Ophthalmic Pack 3_Sterile_8EA/CS FDA UDI
Model / Reference
MEI003 FDA UDI
Description
Ophthalmic Pack 3_Sterile_8EA/CS FDA UDI

Identifiers

Primary DI / UDI-DI
16931918155982 FDA UDI
FDA Product Code
OJK FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4790 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General surgical procedure kit, non-medicated, single-use

Invenio by GRI Medical & Electronic Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
GRI Medical & Electronic Technology Co., Ltd.

Sources (1)

  • FDA UDI 05c80bc1-2039-4a5a-8a1f-829079ff82a0 34 fields · synced Oct 6, 2026