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Toe Crest Pad Sm Lt 3/Pk

FDA UDI

Class I (US FDA UDI)

by Bird & Cronin, Llc

Identity

Trade Name
TOE CREST PAD SM LT 3/PK FDA UDI
Generic Name
Toe separator FDA UDI
Model / Reference
48458152 FDA UDI

Identifiers

Primary DI / UDI-DI
00610570034635 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Toe separator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Toe separator

Toe Crest Pad Sm Lt 3/Pk by Bird & Cronin, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Toe separator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bird & Cronin, Llc

Sources (1)

  • FDA UDI 0cc6146a-0502-4e1c-9a63-9e7aeb1c9110 32 fields · synced May 30, 2026