← Back to catalogue

Oral Syringe

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Oral Syringe FDA UDI
Generic Name
ENFit oral/enteral syringe, single-use FDA UDI
Device Name
12mL Oral Syringe Purp Sterile FDA UDI
Model / Reference
PNM-S12EO FDA UDI
Description
12mL Oral Syringe Purp Sterile FDA UDI

Identifiers

Catalog Number
PNM-S12EO FDA UDI
Primary DI / UDI-DI
00350770002712 FDA UDI
510(k) Number
K122373 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
ENFit oral/enteral syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: ENFit oral/enteral syringe, single-use

Oral Syringe by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENFit oral/enteral syringe, single-use.

Cleared under the same submission

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

Sources (1)

  • FDA UDI d0fe7c0c-2489-47c5-846d-494d30a75f89 36 fields · synced Jun 9, 2026