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Plasdent

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Plasdent FDA UDI
Generic Name
Surgical gown, reusable FDA UDI
Device Name
Supreme Reusable Gown, White FDA UDI
Model / Reference
7004C-1 FDA UDI
Description
Supreme Reusable Gown, White FDA UDI

Identifiers

Catalog Number
7004C-1 FDA UDI
Primary DI / UDI-DI
D8327004C10 FDA UDI
FDA Product Code
OEA FDA UDI
GMDN Term
Surgical gown, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical gown, reusable

Plasdent by Plasdent Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical gown, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI 10e8f77e-6f00-403c-b3e5-7341ca69ff2d 34 fields · synced May 30, 2026