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Rigid Endoscopic Needle

FDA UDI

Class II (US FDA UDI)

by Uroplasty, LLC

Identity

Trade Name
Rigid Endoscopic Needle FDA UDI
Generic Name
General-purpose endoscopic needle, single-use FDA UDI
Model / Reference
MRN-420 FDA UDI

Identifiers

Catalog Number
MRN-420 FDA UDI
Primary DI / UDI-DI
08717591240280 FDA UDI
510(k) Number
K121337 FDA UDI
FDA Product Code
FBK FDA UDI
GMDN Term
General-purpose endoscopic needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

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

Dimensions & Sizes

Size
Needle Gauge — 20 Gauge FDA UDI

Category: General-purpose endoscopic needle, single-use

Rigid Endoscopic Needle by Uroplasty, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose endoscopic needle, single-use.

Cleared under the same submission

K121337 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Uroplasty, LLC

Sources (1)

  • FDA UDI 8f8b8b14-0743-49fa-a5d3-a7da279f28a8 36 fields · synced Jun 8, 2026