← Back to catalogue

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 Hygiene Pack X40 FDA UDI
Model / Reference
8884 FDA UDI
Description
Instrapac Dental Hygiene Pack X40 FDA UDI

Identifiers

Catalog Number
8884 FDA UDI
Primary DI / UDI-DI
05010058088849 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

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

Manufacturer

Manufacturer
Robinson Healthcare Limited

Sources (1)

  • FDA UDI a5783a6b-8ba7-4589-a6b9-d4a2743186ae 36 fields · synced May 30, 2026