← Back to catalogue

Grace Medical, Inc.

FDA UDI

Class I (US FDA UDI)

by Directmed, Inc.

Identity

Trade Name
Grace Medical, Inc. FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
OTOMED® SUCTION TUBING FDA UDI
Model / Reference
SP-4000 FDA UDI
Description
OTOMED® SUCTION TUBING FDA UDI

Identifiers

Primary DI / UDI-DI
00850038863197 FDA UDI
FDA Product Code
GBX FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use 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

Yes

FDA UDI

Category: Surgical irrigation tubing set, single-use

Grace Medical, Inc. by Directmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation tubing set, single-use.

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
Directmed, Inc.

Sources (1)

  • FDA UDI f00593bb-d8c8-40b9-a0f2-416b568b1e37 33 fields · synced May 30, 2026