← Back to catalogue

Captivator™ COLD

FDA UDI

Class I (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Captivator™ COLD FDA UDI
Generic Name
Mechanical-cutting endoscopic polypectomy snare FDA UDI
Device Name
Single-Use Snare FDA UDI
Model / Reference
M00561100 FDA UDI
Description
Single-Use Snare FDA UDI

Identifiers

Primary DI / UDI-DI
08714729971252 FDA UDI
FDA Product Code
FGX FDA UDI
GMDN Term
Mechanical-cutting endoscopic polypectomy snare FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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: Mechanical-cutting endoscopic polypectomy snare

Captivator™ COLD by Boston Scientific — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mechanical-cutting endoscopic polypectomy snare.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 3f7222e9-e4d1-4af9-b2e3-3e1b244b2d97 34 fields · synced Jun 6, 2026