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Lower Seal For Mictec Glass Bottle

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
LOWER SEAL FOR MICTEC GLASS BOTTLE FDA UDI
Generic Name
Surgical suction system collection container, reusable FDA UDI
Device Name
LOWER SEAL FOR MICTEC GLASS BOTTLE FDA UDI
Model / Reference
15-11181-20 FDA UDI
Description
LOWER SEAL FOR MICTEC GLASS BOTTLE FDA UDI

Identifiers

Primary DI / UDI-DI
00192896000117 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Surgical suction system collection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical suction system collection container, reusable

Lower Seal For Mictec Glass Bottle by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 096f1819-7efb-4687-a17b-d5a6aba30545 36 fields · synced May 31, 2026