← Back to catalogue

Hygitech

FDA UDI

Class I (US FDA UDI)

by Hygitech

Identity

Trade Name
HYGITECH FDA UDI
Generic Name
Surgical dressing/drape kit, single-use FDA UDI
Device Name
Standard quality : White, soft, high quality wadding paper towel FDA UDI
Model / Reference
HY-70115 FDA UDI
Description
Standard quality : White, soft, high quality wadding paper towel FDA UDI

Identifiers

Catalog Number
HY-70115 FDA UDI
Primary DI / UDI-DI
03615140003476 FDA UDI
FDA Product Code
FXP FDA UDI
GMDN Term
Surgical dressing/drape kit, 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical dressing/drape kit, single-use

Hygitech by Hygitech — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical dressing/drape kit, 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

Manufacturer
Hygitech

Sources (1)

  • FDA UDI a0659f08-8798-470e-83d9-31001faa21b9 34 fields · synced May 30, 2026