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Hygitech

FDA UDI

Class II (US FDA UDI)

by Hygitech

Identity

Trade Name
HYGITECH FDA UDI
Generic Name
Surgical dressing/drape kit, single-use FDA UDI
Device Name
Cover the patient and keep his eyes uncovered. U-shaped cutout on the shorter side with adhesive for easy positioning and fixing around the collar. Size of the U cutout: diameter 11.5 cm, height 10 cm. FDA UDI
Model / Reference
HY-60010 FDA UDI
Description
Cover the patient and keep his eyes uncovered. U-shaped cutout on the shorter side with adhesive for easy positioning and fixing around the collar. Size of the U cutout: diameter 11.5 cm, height 10 cm. FDA UDI

Identifiers

Catalog Number
HY-60010 FDA UDI
Primary DI / UDI-DI
03615140003506 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Surgical dressing/drape kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

No

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 II — 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 390c7eee-f775-4442-9dd2-1181c89bf6c0 34 fields · synced May 31, 2026