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Puritan Opti-Swab

FDA UDI

Class I (US FDA UDI)

by Puritan Medical Products Company Llc

Identity

Trade Name
Puritan Opti-Swab FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, single-use FDA UDI
Device Name
Puritan Fecal Opti-Swab Collection & Transport System FDA UDI
Model / Reference
CB-206 (25-3506-H) FDA UDI
Description
Puritan Fecal Opti-Swab Collection & Transport System FDA UDI

Identifiers

Catalog Number
CB-206 (25-3506-H) FDA UDI
Primary DI / UDI-DI
30609576900892 FDA UDI
FDA Product Code
JSM FDA UDI
GMDN Term
General-purpose absorbent tip applicator/swab, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2390 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

No

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 Opti-Swab 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 21aa047b-6ca4-4d25-be90-fa4c59c585ea 36 fields · synced Jun 8, 2026