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Intussusception Air Reduction Bulb & Gauge with Plastic Case

FDA UDI

Class II (US FDA UDI)

by Gri Medical Products, Inc.

Identity

Trade Name
Intussusception Air Reduction Bulb & Gauge with Plastic Case FDA UDI
Generic Name
Gravity enema set FDA UDI
Device Name
Intussusception Air Reduction Bulb & Gauge with Plastic Case FDA UDI
Model / Reference
IARB-KIT FDA UDI
Description
Intussusception Air Reduction Bulb & Gauge with Plastic Case FDA UDI

Identifiers

Catalog Number
IARB-KIT FDA UDI
Primary DI / UDI-DI
00860002476148 FDA UDI
FDA Product Code
KQT FDA UDI
GMDN Term
Gravity enema set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gravity enema set

Intussusception Air Reduction Bulb & Gauge with Plastic Case by Gri Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Gravity enema set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 86328b05-6cb1-4615-8e8e-b773793f9b72 34 fields · synced Jun 1, 2026