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Coblation

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Coblation FDA UDI
Generic Name
Arthroscopic irrigation/insufflation system FDA UDI
Device Name
SAP TUBE CLIP FDA UDI
Model / Reference
E3030-01 FDA UDI
Description
SAP TUBE CLIP FDA UDI

Identifiers

Catalog Number
E3030-01 FDA UDI
Primary DI / UDI-DI
20817470008993 FDA UDI
510(k) Number
K122652 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Arthroscopic irrigation/insufflation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arthroscopic irrigation/insufflation system

Coblation by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic irrigation/insufflation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 21449343-ed11-4d11-b681-b348f6f4be92 36 fields · synced Jun 8, 2026