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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 waterproof absorbent surgical drape. Sterile dual layered surgical drape, absorbent and impermeable, ensures the best protection! Protects the equipment, tables and the patient's chest and shoulders. FDA UDI
Model / Reference
HY-525 FDA UDI
Description
Standard waterproof absorbent surgical drape. Sterile dual layered surgical drape, absorbent and impermeable, ensures the best protection! Protects the equipment, tables and the patient's chest and shoulders. FDA UDI

Identifiers

Catalog Number
HY-525 FDA UDI
Primary DI / UDI-DI
03615140003094 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

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

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 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

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Manufacturer

Manufacturer
Hygitech

Sources (1)

  • FDA UDI ec227607-4e47-4c91-b217-663f7a50b095 34 fields · synced May 31, 2026