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Instrapac

FDA UDI

Class I (US FDA UDI)

by Robinson Healthcare Limited

Identity

Trade Name
Instrapac FDA UDI
Generic Name
General surgery wound probe/packer FDA UDI
Device Name
Instrapac Silver Probe with Eye 13cm X 50 FDA UDI
Model / Reference
7899 FDA UDI
Description
Instrapac Silver Probe with Eye 13cm X 50 FDA UDI

Identifiers

Catalog Number
7899 FDA UDI
Primary DI / UDI-DI
05010058078994 FDA UDI
FDA Product Code
KDC FDA UDI
GMDN Term
General surgery wound probe/packer 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 13 Centimeter FDA UDI

Category: General surgery wound probe/packer

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

Similar devices

Also classified as General surgery wound probe/packer.

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 d267fd21-e3e6-460b-9ee9-a0ec95635e6c 37 fields · synced Jun 6, 2026