← Back to catalogue

Connector Holder Kit

FDA UDI

Class III (US FDA UDI)

by Synapse Biomedical, Inc.

Identity

Trade Name
Connector Holder Kit FDA UDI
Generic Name
Intramuscular diaphragm/phrenic nerve electrical stimulation system FDA UDI
Model / Reference
22-0004 FDA UDI

Identifiers

Primary DI / UDI-DI
00852184003342 FDA UDI
FDA Product Code
OIR FDA UDI
GMDN Term
Intramuscular diaphragm/phrenic nerve electrical stimulation system FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intramuscular diaphragm/phrenic nerve electrical stimulation system

Connector Holder Kit by Synapse Biomedical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intramuscular diaphragm/phrenic nerve electrical stimulation system.

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
Synapse Biomedical, Inc.

Sources (1)

  • FDA UDI 3c894a82-99f7-4fbf-840f-201e776dfe2d 32 fields · synced May 30, 2026