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Wishbone Mg

FDA UDI

Class II (US FDA UDI)

by Wishbone Medical Inc.

Identity

Trade Name
WISHBONE MG FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
MIXING AND DELIVERY SYSTEM FDA UDI
Model / Reference
PK-BVF00 FDA UDI
Description
MIXING AND DELIVERY SYSTEM FDA UDI

Identifiers

Primary DI / UDI-DI
B562PKBVF000 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic surgical procedure kit, non-medicated, single-use

Wishbone Mg by Wishbone Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wishbone Medical Inc.

Sources (1)

  • FDA UDI fa076bfa-e66f-44ac-9967-6aafb0053aca 33 fields · synced May 31, 2026