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Neonatal Starter Set

FDA UDI

Class II (US FDA UDI)

by Sentec, Inc.

Identity

Trade Name
Neonatal Starter Set FDA UDI
Generic Name
Transcutaneous blood gas monitoring system FDA UDI
Device Name
Neonatal Starter Set contains: Multi-Site Attachment Rings for mature/intact skin (MAR-MI) Multi-Site Attachment Rings for sensitive/fragile skin (MAR-SF) Membrane Changer tool (reloadable) (MC-R) Contact Gel (GEL-04) Service Gas (GAS-0812) FDA UDI
Model / Reference
SSET-N FDA UDI
Description
Neonatal Starter Set contains: Multi-Site Attachment Rings for mature/intact skin (MAR-MI) Multi-Site Attachment Rings for sensitive/fragile skin (MAR-SF) Membrane Changer tool (reloadable) (MC-R) Contact Gel (GEL-04) Service Gas (GAS-0812) FDA UDI

Identifiers

Primary DI / UDI-DI
07640121880438 FDA UDI
510(k) Number
K041548 FDA UDI
K071672 FDA UDI
K101690 FDA UDI
K151329 FDA UDI
FDA Product Code
DPZ FDA UDI
DQA FDA UDI
KLK FDA UDI
LKD FDA UDI
LPP FDA UDI
GMDN Term
Transcutaneous blood gas monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2710 FDA UDI
870.2700 FDA UDI
868.2500 FDA UDI
868.2480 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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

Neonatal Starter Set by Sentec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sentec, Inc.

Sources (1)

  • FDA UDI 6d59538c-954b-453c-a3c1-3cb4a54fc101 36 fields · synced Jun 8, 2026