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Grace Medical

FDA UDI

Class I (US FDA UDI)

by Network Medical Products, Ltd.

Identity

Trade Name
Grace Medical FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
Device Name
SSP-017 - Aspiration Cannula Red 1.4mm/17G FDA UDI
Model / Reference
SSP-017 FDA UDI
Description
SSP-017 - Aspiration Cannula Red 1.4mm/17G FDA UDI

Identifiers

Catalog Number
SSP-017 FDA UDI
Primary DI / UDI-DI
05056100706538 FDA UDI
FDA Product Code
JZF FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical/emergency suction cannula, non-illuminating, single-use

Grace Medical by Network Medical Products, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Network Medical Products, Ltd.

Sources (1)

  • FDA UDI 1b8e5412-6e06-4d68-9df9-00e73f2b0831 34 fields · synced Jun 1, 2026