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Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Bone grafting cannula FDA UDI
Device Name
SYRINGE GRAFT DELIVERY CURVED W/FUNNEL SS 4.5MM OPENING HOLDS APPROX 2.1CC OF MATERIAL FDA UDI
Model / Reference
9800045 FDA UDI
Description
SYRINGE GRAFT DELIVERY CURVED W/FUNNEL SS 4.5MM OPENING HOLDS APPROX 2.1CC OF MATERIAL FDA UDI

Identifiers

Catalog Number
9800045 FDA UDI
Primary DI / UDI-DI
00614950016495 FDA UDI
FDA Product Code
EIC FDA UDI
GMDN Term
Bone grafting cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone grafting cannula

Ace by Ace Surgical Supply Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone grafting cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e83858c-8d1e-46d3-9fb1-45aa2e0ee3b5 36 fields · synced May 29, 2026