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Puritan

FDA UDI

Class I (US FDA UDI)

by Puritan Medical Products Company Llc

Identity

Trade Name
Puritan FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, single-use FDA UDI
Device Name
Sterile Polyester Tipped Applicators FDA UDI
Model / Reference
25-806 1PDB 1500 FDA UDI
Description
Sterile Polyester Tipped Applicators FDA UDI

Identifiers

Catalog Number
25-806 1PDB 1500 FDA UDI
Primary DI / UDI-DI
00609576381508 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

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

No

FDA UDI

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

Puritan by Puritan Medical Products Company Llc — 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

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Manufacturer

Sources (1)

  • FDA UDI 594b45a4-0328-4315-be4f-ec995a788524 35 fields · synced May 29, 2026