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Invenio

FDA UDI

Class I (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
Invenio FDA UDI
Generic Name
Absorbent underpad, non-antimicrobial, single-use FDA UDI
Device Name
Body Bag Liner Sheet_bulk package 20ea/cs FDA UDI
Model / Reference
i60-BL3072 FDA UDI
Description
Body Bag Liner Sheet_bulk package 20ea/cs FDA UDI

Identifiers

Primary DI / UDI-DI
16931918137704 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Absorbent underpad, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Absorbent underpad, non-antimicrobial, single-use

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

Similar devices

Also classified as Absorbent underpad, non-antimicrobial, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82b5b159-024d-46bf-993b-45822f1133c8 34 fields · synced Sep 18, 2026