← Back to catalogue

National Hospital Packaging

FDA UDI

Class I (US FDA UDI)

by Surgi-Pak, Inc.

Identity

Trade Name
NATIONAL HOSPITAL PACKAGING FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, single-use FDA UDI
Device Name
COTTON TIPPED APPLICATORS, 3IN, 18/PKG, STRL FDA UDI
Model / Reference
13-003 FDA UDI
Description
COTTON TIPPED APPLICATORS, 3IN, 18/PKG, STRL FDA UDI

Identifiers

Catalog Number
13-003 FDA UDI
Primary DI / UDI-DI
00817213020394 FDA UDI
FDA Product Code
KXG FDA UDI
GMDN Term
General-purpose absorbent tip applicator/swab, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6025 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose absorbent tip applicator/swab, single-use

National Hospital Packaging by Surgi-Pak, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose absorbent tip applicator/swab, 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
Surgi-Pak, Inc.

Sources (1)

  • FDA UDI e9e1a01e-78c6-41cb-967d-8954016cc2e8 35 fields · synced Jun 6, 2026