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Lee Medical

FDA UDI

Class I (US FDA UDI)

by Tarca LLC

Identity

Trade Name
Lee Medical FDA UDI
Generic Name
Body aspiration needle, single-use FDA UDI
Device Name
Adult - Long LEE ® Bone Marrow Aspiration Needle 15 Gauge – 4 inch (101mm) FDA UDI
Model / Reference
A-154 FDA UDI
Description
Adult - Long LEE ® Bone Marrow Aspiration Needle 15 Gauge – 4 inch (101mm) FDA UDI

Identifiers

Catalog Number
A-154 FDA UDI
Primary DI / UDI-DI
00850048404014 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Body aspiration 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

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

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: Body aspiration needle, single-use

Lee Medical by Tarca LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body aspiration needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tarca LLC

Sources (1)

  • FDA UDI c139ba97-2787-41b1-a1f8-9e0ffd97a141 34 fields · synced May 30, 2026