← Back to catalogue

Medline Pressure Infuser Bag 1000ml

FDA UDI

Class I (US FDA UDI)

by Renu Medical, Inc

Identity

Trade Name
Medline Pressure Infuser Bag 1000ml FDA UDI
Generic Name
Intravenous pressure infusor, manual, single-use FDA UDI
Model / Reference
RM-DYNJAAPI1000B FDA UDI

Identifiers

Primary DI / UDI-DI
00816317024277 FDA UDI
FDA Product Code
KZD FDA UDI
GMDN Term
Intravenous pressure infusor, manual, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intravenous pressure infusor, manual, single-use

Medline Pressure Infuser Bag 1000ml by Renu Medical, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous pressure infusor, manual, 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
Renu Medical, Inc

Sources (1)

  • FDA UDI e35e3a12-70ca-43a2-8423-430af7c4183a 32 fields · synced May 30, 2026