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Individual Ancillary Item Kit

FDA UDI

Class II (US FDA UDI)

by Custom Interventional Pain Management

Identity

Trade Name
Individual Ancillary Item Kit FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Convenience kit non-medicated FDA UDI
Model / Reference
70 FDA UDI
Description
Convenience kit non-medicated FDA UDI

Identifiers

Catalog Number
70 FDA UDI
Primary DI / UDI-DI
B875700 FDA UDI
FDA Product Code
OGD FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5120 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

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: General surgical procedure kit, non-medicated, single-use

Individual Ancillary Item Kit by Custom Interventional Pain Management — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General 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
Custom Interventional Pain Management

Sources (1)

  • FDA UDI 48c2f6d9-b514-4c0e-8f81-ead47d6ba033 34 fields · synced May 30, 2026