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Single Use Aspiration Needle NA2

FDA UDI

Class I (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Single Use Aspiration Needle NA2 FDA UDI
Generic Name
General-purpose endoscopic needle, single-use FDA UDI
Model / Reference
NA-601D-1519 FDA UDI

Identifiers

Primary DI / UDI-DI
04953170216626 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
General-purpose endoscopic needle, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI

Category: General-purpose endoscopic needle, single-use

Single Use Aspiration Needle NA2 by Olympus Medical Systems Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2ffedb3f-8c28-4b25-9170-37d27c0a39ab 33 fields · synced Jun 8, 2026