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Grace Medical T-Tube

FDA UDI

Class II (US FDA UDI)

by Grace Medical, Inc.

Identity

Trade Name
GRACE MEDICAL T-TUBE FDA UDI
Generic Name
Tympanostomy tube FDA UDI
Device Name
T-TUBE 1.14MM ID X 12MM LENGTH SILICONE PAIR 10 PACK FDA UDI
Model / Reference
510-102 FDA UDI
Description
T-TUBE 1.14MM ID X 12MM LENGTH SILICONE PAIR 10 PACK FDA UDI

Identifiers

Primary DI / UDI-DI
00844505003025 FDA UDI
510(k) Number
K981575 FDA UDI
FDA Product Code
ETD FDA UDI
GMDN Term
Tympanostomy tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3880 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Tympanostomy tube

Grace Medical T-Tube by Grace Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tympanostomy tube.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Grace Medical, Inc.

Sources (1)

  • FDA UDI 53147b03-e5c1-4b4d-ac67-eae0021821da 35 fields · synced May 30, 2026