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Avaline Medical NJ LLC

FDA UDI

Class I (US FDA UDI)

by Avaline Medical NJ Limited Liability Company

Identity

Trade Name
Avaline Medical NJ LLC FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, single-use FDA UDI
Device Name
400 Sterile 6" Cotton Tip Applicator FDA UDI
Model / Reference
4305x2+st FDA UDI
Description
400 Sterile 6" Cotton Tip Applicator FDA UDI

Identifiers

Catalog Number
4305x2+st FDA UDI
Primary DI / UDI-DI
00650415208630 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
Not 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

Yes

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

Avaline Medical NJ LLC by Avaline Medical NJ Limited Liability Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 91fd2069-62af-469d-bc31-be5e95bb33f3 36 fields · synced May 30, 2026