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Extended Reservoir™

FDA UDI

Class III (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name
Extended Reservoir™ FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
RSVR MMT-342G 5PK EW 3ML US FDA UDI
Model / Reference
MMT-342G FDA UDI
Description
RSVR MMT-342G 5PK EW 3ML US FDA UDI

Identifiers

Primary DI / UDI-DI
00763000837259 FDA UDI
510(k) Number
K210714 FDA UDI
FDA Product Code
LZP FDA UDI
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
886.4275 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose syringe, single-use

Extended Reservoir™ by Medtronic Minimed, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 55fabf15-bf0c-45e7-a190-1a064f122be5 36 fields · synced May 30, 2026