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Stylet

FDA UDI

Class I (US FDA UDI)

by Medionics International , Ltd.

Identity

Trade Name
Stylet FDA UDI
Generic Name
Peritoneal catheter stylet FDA UDI
Model / Reference
SST-650 FDA UDI

Identifiers

Catalog Number
SST-650 FDA UDI
Primary DI / UDI-DI
00792079000431 FDA UDI
FDA Product Code
GBW FDA UDI
GMDN Term
Peritoneal catheter stylet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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: Peritoneal catheter stylet

Stylet by Medionics International , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peritoneal catheter stylet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bcc9ef7e-1926-49bd-abe6-db7a3060c165 34 fields · synced May 30, 2026