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HK Sterile Super Absorbent Pads Medium

FDA UDI

Class I (US FDA UDI)

by Hk Surgical Inc.

Identity

Trade Name
HK Sterile Super Absorbent Pads Medium FDA UDI
Generic Name
Absorbent wound compression pad FDA UDI
Device Name
HK Sterile Super Absorbent Pads Medium FDA UDI
Model / Reference
SPD-M FDA UDI
Description
HK Sterile Super Absorbent Pads Medium FDA UDI

Identifiers

Catalog Number
SPD-M FDA UDI
Primary DI / UDI-DI
00816989020812 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Absorbent wound compression pad FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

Yes

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: Absorbent wound compression pad

HK Sterile Super Absorbent Pads Medium by Hk Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Absorbent wound compression pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hk Surgical Inc.

Sources (1)

  • FDA UDI c7e87858-7e3d-44a8-ab5b-a7ce42e03590 35 fields · synced May 31, 2026