← Back to catalogue

Copioumed

FDA UDI

Class I (US FDA UDI)

by Copious International Inc.

Identity

Trade Name
Copioumed FDA UDI
Generic Name
Surgical cap, single-use FDA UDI
Device Name
Copioumed The tie-band headwear is made of non-woven fabric, which is made by cutting and sewing. It is non-sterile and disposable. FDA UDI
Model / Reference
SCN0B181-1 FDA UDI
Description
Copioumed The tie-band headwear is made of non-woven fabric, which is made by cutting and sewing. It is non-sterile and disposable. FDA UDI

Identifiers

Primary DI / UDI-DI
04719882253560 FDA UDI
FDA Product Code
FYF FDA UDI
GMDN Term
Surgical cap, single-use 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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: Surgical cap, single-use

Copioumed by Copious International Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical cap, 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 7aa20ccd-c659-4312-86bb-a0bc5ec0b7e2 34 fields · synced May 30, 2026