Front1 Health Partners

FDA UDI

Class I (US FDA UDI)

by Degania Silicone Ltd

Identity

Trade Name: Front1 Health Partners FDA UDI
Generic Name: Surgical capillary wound drain, non-luminal FDA UDI
Device Name: Straight silicone wound drain 32Fr FDA UDI
Model / Reference: 11006803280F1 FDA UDI
Description: Straight silicone wound drain 32Fr FDA UDI

Identifiers

Primary DI / UDI-DI: 07290110066017 FDA UDI
FDA Product Code: GBS FDA UDI
GMDN Term: Surgical capillary wound drain, non-luminal FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Surgical capillary wound drain, non-luminal

Front1 Health Partners by Degania Silicone Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical capillary wound drain, non-luminal.

MICROMAT® — Pmt Corp. · Class II
MICROMAT® — Pmt Corp. · Class II
MICROMAT® — Pmt Corp. · Class II
MICROMAT® — Pmt Corp. · Class II
MICROMAT® — Pmt Corp. · Class II
MICROMAT® — Pmt Corp. · Class II
MICROMAT® — Pmt Corp. · Class II
MICROMAT® — Pmt Corp. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Degania Silicone Ltd

Sources (1)

FDA UDI 1085a8da-7bda-4c1a-8018-461e341e0d2e 33 fields · synced Jun 1, 2026