← Back to catalogue

Wrist Hand Orthosis Md Rt

FDA UDI

Class I (US FDA UDI)

by Bird & Cronin, Llc

Identity

Trade Name
WRIST HAND ORTHOSIS MD RT FDA UDI
Generic Name
Wrist/hand orthosis FDA UDI
Model / Reference
08147323 FDA UDI

Identifiers

Primary DI / UDI-DI
00610570104550 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Wrist/hand 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: Wrist/hand orthosis

Wrist Hand Orthosis Md Rt by Bird & Cronin, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wrist/hand orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bird & Cronin, Llc

Sources (1)

  • FDA UDI db6ae693-8358-48d9-8592-7a67f742dfce 32 fields · synced May 30, 2026