← Back to catalogue

Keystone Sterile Specimen Collection Polyester Swab - 6 inch

FDA UDI

Class I (US FDA UDI)

by Keystone Manufacturing

Identity

Trade Name
Keystone Sterile Specimen Collection Polyester Swab - 6 inch FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, single-use FDA UDI
Device Name
Sterile Specimen Collection Sterile Polyester Swab - 6 inch FDA UDI
Model / Reference
KMSWAB-806P-100 FDA UDI
Description
Sterile Specimen Collection Sterile Polyester Swab - 6 inch FDA UDI

Identifiers

Primary DI / UDI-DI
00860003793718 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

Keystone Sterile Specimen Collection Polyester Swab - 6 inch by Keystone Manufacturing — 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

Sources (1)

  • FDA UDI 87fb5280-0261-490a-a103-4f4fcbf4faca 33 fields · synced May 31, 2026