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FastForward

FDA UDI

Class II (US FDA UDI)

by Medshape, Inc.

Identity

Trade Name
FastForward FDA UDI
Generic Name
Orthopaedic bone washer, sterile FDA UDI
Device Name
Plate, FastForward, Medium FDA UDI
Model / Reference
1700-00-001 FDA UDI
Description
Plate, FastForward, Medium FDA UDI

Identifiers

Primary DI / UDI-DI
M9701700000010 FDA UDI
FDA Product Code
HTN FDA UDI
GMDN Term
Orthopaedic bone washer, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

No

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic bone washer, sterile

FastForward by Medshape, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone washer, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medshape, Inc.

Sources (1)

  • FDA UDI d38d7da4-4efd-4f47-b4d7-9481b0abb17e 33 fields · synced May 30, 2026