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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
Limb/torso/head restraint, single-use FDA UDI
Device Name
VELCRO STRAP 1X12" W/BUCKLE L/F FDA UDI
Model / Reference
0031012 FDA UDI
Description
VELCRO STRAP 1X12" W/BUCKLE L/F FDA UDI

Identifiers

Catalog Number
0031012 FDA UDI
Primary DI / UDI-DI
00614950013050 FDA UDI
FDA Product Code
KID FDA UDI
GMDN Term
Limb/torso/head restraint, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3910 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

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

Dimensions & Sizes

Size
Length — 12 Inch FDA UDI

Category: Limb/torso/head restraint, single-use

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

Similar devices

Also classified as Limb/torso/head restraint, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ace Surgical Supply Co., Inc.

Sources (1)

  • FDA UDI ef0151bd-88c2-4d89-bc7b-f9eb2d446721 37 fields · synced Jun 8, 2026