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HydroSeal™

FDA UDI

Class I (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name
HydroSeal™ FDA UDI
Generic Name
Arthroscopic access cannula, single-use FDA UDI
Device Name
HydroSeal™ Silicone Cannula 12mm x 40mm FDA UDI
Model / Reference
HS-1240 FDA UDI
Description
HydroSeal™ Silicone Cannula 12mm x 40mm FDA UDI

Identifiers

Catalog Number
148124cn FDA UDI
Primary DI / UDI-DI
30810128461031 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Arthroscopic access cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Arthroscopic access cannula, single-use

HydroSeal™ by T.a.g Medical Products Agricultural Cooperative Association — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic access cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 72e0ec1c-a74b-409a-8b0d-1dda02bbf2e7 34 fields · synced May 31, 2026