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Instrapac

FDA UDI

Class I (US FDA UDI)

by Robinson Healthcare Limited

Identity

Trade Name
Instrapac FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Instrapac Dental Conservation Pack x 40 FDA UDI
Model / Reference
7123 FDA UDI
Description
Instrapac Dental Conservation Pack x 40 FDA UDI

Identifiers

Catalog Number
7123 FDA UDI
Primary DI / UDI-DI
05010058071230 FDA UDI
FDA Product Code
NYC FDA UDI
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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: Dental/maxillofacial surgical procedure kit, non-medicated, single-use

Instrapac by Robinson Healthcare Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental/maxillofacial 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
Robinson Healthcare Limited

Sources (1)

  • FDA UDI 0e9e9d8d-ea8d-4fef-82b9-a32a4c6fa3f2 36 fields · synced Jun 6, 2026