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Graft Material Spatula / Carrier

FDA UDI

Class I (US FDA UDI)

by W.H. Holden, Inc.

Identity

Trade Name
GRAFT MATERIAL SPATULA / CARRIER FDA UDI
Generic Name
Bone graft syringe, reusable FDA UDI
Model / Reference
70-6262 FDA UDI

Identifiers

Primary DI / UDI-DI
D9287062620 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Bone graft syringe, reusable 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone graft syringe, reusable

Graft Material Spatula / Carrier by W.H. Holden, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone graft syringe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W.H. Holden, Inc.

Sources (1)

  • FDA UDI 5253263a-fc66-4e0e-962f-11ffc25159a5 32 fields · synced Jun 8, 2026