← Back to catalogue

Flexision

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 490102

by Intuitive Surgical, Inc.

Identity

Trade Name
Flexision Biopsy Needle, 23G EUDAMED
Flexision FDA UDI
Generic Name
General-purpose endoscopic needle, single-use FDA UDI
Device Name
Ion Biopsy Needle EUDAMED
Biopsy Needle, 23G FDA UDI
Model / Reference
490102 EUDAMEDFDA UDI
Description
Biopsy Needle, 23G FDA UDI

Identifiers

Primary DI / UDI-DI
00886874115954 EUDAMEDFDA UDI
Basic UDI-DI
08868741211397V EUDAMED
FDA Product Code
EOQ FDA UDI
EMDN Code
A010299 BIOPSY NEEDLES AND KITS - OTHER EUDAMED
GMDN Term
General-purpose endoscopic needle, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
874.4680 FDA UDI
Medical Purpose
The Flexision Biopsy Needle is intended to retrieve tissue from a target structure. EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA 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

Category: General-purpose endoscopic needle, single-use

Flexision by Intuitive Surgical, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 5ba83bc7-fece-4bf0-80ec-aaa4180e12e8 33 fields · synced Jul 23, 2026
  • EUDAMED 4bc53c7c-62f5-4a13-8cb3-6124e8054058 61 fields · synced Jul 23, 2026