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Stand Alone

FDA UDI

Class I (US FDA UDI)

by Newclip Technics

Identity

Trade Name
Stand Alone FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Model / Reference
KIT-SCQ4.0 FDA UDI

Identifiers

Catalog Number
KIT-SCQ4.0 FDA UDI
Primary DI / UDI-DI
03700569634285 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

Stand Alone by Newclip Technics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Newclip Technics

Sources (1)

  • FDA UDI 0be2ad10-d6a8-42ff-8386-eeb98658bd77 33 fields · synced May 30, 2026