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Sterling Healthcare Manufacturing

FDA UDI

Class I (US FDA UDI)

by The Rodon Group

Identity

Trade Name
Sterling Healthcare Manufacturing FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, single-use FDA UDI
Device Name
Sterling Fluid Trap-Tip Swabs, Sterile, Flexible Stem FDA UDI
Model / Reference
4027 FDA UDI
Description
Sterling Fluid Trap-Tip Swabs, Sterile, Flexible Stem FDA UDI

Identifiers

Primary DI / UDI-DI
00860005875511 FDA UDI
FDA Product Code
KXF 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Sterling Healthcare Manufacturing by The Rodon Group — 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

Manufacturer
The Rodon Group

Sources (1)

  • FDA UDI 2b0e6993-4612-4e6d-aba7-3929a1974971 33 fields · synced May 30, 2026