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Platypus

FDA UDI

Class I (US FDA UDI)

by Inspiration G5 LLC dba PlatypusCo

Identity

Trade Name
Platypus FDA UDI
Generic Name
Dental floss FDA UDI
Device Name
Platypus T103 Patient Sample Pack includes 75 3-count flossers. FDA UDI
Model / Reference
T103 FDA UDI
Description
Platypus T103 Patient Sample Pack includes 75 3-count flossers. FDA UDI

Identifiers

Primary DI / UDI-DI
00858813002038 FDA UDI
FDA Product Code
JES FDA UDI
GMDN Term
Dental floss FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6390 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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: Dental floss

Platypus by Inspiration G5 LLC dba PlatypusCo — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental floss.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ef686838-5851-4019-99ba-a792f8669215 33 fields · synced May 30, 2026