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Bvi

FDA UDI

Class II (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
BVI FDA UDI
Generic Name
Surgical gown, single-use FDA UDI
Device Name
Surgical Gown_Non-Reinforced_W/ one hand towle_S_Non-Sterile_28ea/cs FDA UDI
Model / Reference
60300469 FDA UDI
Description
Surgical Gown_Non-Reinforced_W/ one hand towle_S_Non-Sterile_28ea/cs FDA UDI

Identifiers

Primary DI / UDI-DI
16931918142777 FDA UDI
510(k) Number
K102652 FDA UDI
FDA Product Code
FYA FDA UDI
GMDN Term
Surgical gown, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical gown, single-use

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

Similar devices

Also classified as Surgical gown, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8f72700e-28d4-490d-a5f9-5bde627d8ffc 35 fields · synced Sep 18, 2026