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Atticus cotton carrier

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Atticus cotton carrier FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, reusable FDA UDI
Device Name
extra fine, serrated Ø 0.8 mm, 11 cm, 5 pieces/box FDA UDI
Model / Reference
10-205-04 FDA UDI
Description
extra fine, serrated Ø 0.8 mm, 11 cm, 5 pieces/box FDA UDI

Identifiers

Catalog Number
10-205-04 FDA UDI
Primary DI / UDI-DI
04250676735010 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
General-purpose absorbent tip applicator/swab, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose absorbent tip applicator/swab, reusable

Atticus cotton carrier by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose absorbent tip applicator/swab, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spiggle & Theis Medizintechnik GmbH

Sources (1)

  • FDA UDI 97216c2d-9ad8-4711-b035-f633f613ab7f 35 fields · synced May 30, 2026