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Tube-Stat®

FDA UDI

Class I (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
TUBE-STAT® FDA UDI
Generic Name
Rigid intubation laryngoscope, reusable FDA UDI
Device Name
STYLET 8330410 TUBE-STAT NASO-TRACH ROHS FDA UDI
Model / Reference
8330410 FDA UDI
Description
STYLET 8330410 TUBE-STAT NASO-TRACH ROHS FDA UDI

Identifiers

Primary DI / UDI-DI
00643169457188 FDA UDI
510(k) Number
K843490 FDA UDI
FDA Product Code
BSR FDA UDI
GMDN Term
Rigid intubation laryngoscope, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5790 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Tube-Stat® by Medtronic Xomed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e69b3462-ae63-48a5-9aac-c8553d64aae8 36 fields · synced Jun 8, 2026