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Celling Biosciences Aspiration and Delivery System

FDA UDI

Class II (US FDA UDI)

by Celling Biosciences

Identity

Trade Name
Celling Biosciences Aspiration and Delivery System FDA UDI
Generic Name
Bone graft syringe, single-use FDA UDI
Device Name
Celling Biosciences Aspiration Needle, 11GA x 11cm - DO NO TUSE - UDI INCORRECT - See UDI# 00817771029440 FDA UDI
Model / Reference
1305-1143 FDA UDI
Description
Celling Biosciences Aspiration Needle, 11GA x 11cm - DO NO TUSE - UDI INCORRECT - See UDI# 00817771029440 FDA UDI

Identifiers

Catalog Number
1305-1143 FDA UDI
Primary DI / UDI-DI
00817771029860 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone graft syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 FDA UDI
Commercial Distribution
Not 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

Celling Biosciences Aspiration and Delivery System by Celling Biosciences — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Celling Biosciences

Sources (1)

  • FDA UDI 1113e5f3-8816-4b78-9c83-000325a96302 36 fields · synced May 30, 2026