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Acquire™ S

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Acquire™ S FDA UDI
Generic Name
General-purpose endoscopic needle, single-use FDA UDI
Device Name
Endoscopic Ultrasound Fine Needle Biopsy (FNB) Device FDA UDI
Model / Reference
M00555660 FDA UDI
Description
Endoscopic Ultrasound Fine Needle Biopsy (FNB) Device FDA UDI

Identifiers

Catalog Number
M00555660 FDA UDI
Primary DI / UDI-DI
00191506030759 FDA UDI
FDA Product Code
ODG 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 25 Gauge FDA UDI

Category: General-purpose endoscopic needle, single-use

Acquire™ S by Boston Scientific — Class II — 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

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 27edd7f0-c237-400d-a5a7-df2d993d1d8c 35 fields · synced May 30, 2026