← Back to catalogue

Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Maxillofacial bone wire/bar FDA UDI
Device Name
WIRE 28G SS 4OZ SPOOL AUTOCLAVABLE DELRIN .0126" FDA UDI
Model / Reference
0800087 FDA UDI
Description
WIRE 28G SS 4OZ SPOOL AUTOCLAVABLE DELRIN .0126" FDA UDI

Identifiers

Catalog Number
0800087 FDA UDI
Primary DI / UDI-DI
00614950022519 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Maxillofacial bone wire/bar FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

Yes

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: Maxillofacial bone wire/bar

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

Similar devices

Also classified as Maxillofacial bone wire/bar.

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

Manufacturer
Ace Surgical Supply Co., Inc.

Sources (1)

  • FDA UDI fcb7d84d-67e1-4019-affc-db9efd444fa4 36 fields · synced May 30, 2026