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Fluid Management Pack

FDA UDI

Class I (US FDA UDI)

by Obp Corporation

Identity

Trade Name
FLUID MANAGEMENT PACK FDA UDI
Generic Name
Urological surgical procedure kit, medicated, single-use FDA UDI
Model / Reference
C050100 FDA UDI

Identifiers

Catalog Number
C050100 FDA UDI
Primary DI / UDI-DI
M648C0501000 FDA UDI
FDA Product Code
NWW FDA UDI
GMDN Term
Urological surgical procedure kit, medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1690 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

No

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

Category: Urological surgical procedure kit, medicated, single-use

Fluid Management Pack by Obp Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urological surgical procedure kit, medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Obp Corporation

Sources (1)

  • FDA UDI 3e8ab1d8-0c23-4d8e-80a1-6689aa902fb8 34 fields · synced May 30, 2026