← Back to catalogue

Spunlace Regular Surgical Gown (Sterile)-M

FDA UDI

Class II (US FDA UDI)

by Medtecs (taiwan) Corp.

Identity

Trade Name
Spunlace Regular Surgical Gown (Sterile)-M FDA UDI
Generic Name
Surgical gown, single-use FDA UDI
Device Name
The SPUNLACE Regular Gown is a device that is intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from transfer of microorganisms, body fluids, and particulate material. The SPUNLACE Regular Gown is made from SPUNLACE material, and is full length, constructed with raglan sleeves, hook and loop neck closures, and tie waist closures. The gowns come with sterile. FDA UDI
Model / Reference
JCSG80100M FDA UDI
Description
The SPUNLACE Regular Gown is a device that is intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from transfer of microorganisms, body fluids, and particulate material. The SPUNLACE Regular Gown is made from SPUNLACE material, and is full length, constructed with raglan sleeves, hook and loop neck closures, and tie waist closures. The gowns come with sterile. FDA UDI

Identifiers

Primary DI / UDI-DI
04710415369185 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

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

Yes

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

Spunlace Regular Surgical Gown (Sterile)-M by Medtecs (taiwan) Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical gown, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 93c649ce-9c21-481b-9e1e-53c29ecd3e37 33 fields · synced Jun 6, 2026