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Ankle Brace Stirrup Sm

FDA UDI

Class I (US FDA UDI)

by Bird & Cronin, Llc

Identity

Trade Name
ANKLE BRACE STIRRUP SM FDA UDI
Generic Name
Ankle/foot orthosis FDA UDI
Model / Reference
AB2351-00 FDA UDI

Identifiers

Primary DI / UDI-DI
00610570176038 FDA UDI
FDA Product Code
ITW FDA UDI
GMDN Term
Ankle/foot orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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: Ankle/foot orthosis

Ankle Brace Stirrup Sm by Bird & Cronin, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

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 b94a76cb-049b-4d26-b8fa-f66ff4f54c29 32 fields · synced Jun 1, 2026