Alistrap Maxx 10 In Wide X 30ft Long

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name: ALISTRAP MAXX 10 IN WIDE X 30FT LONG FDA UDI
Generic Name: Limb/torso/head restraint, reusable FDA UDI
Model / Reference: 95-908 FDA UDI

Identifiers

Catalog Number: 2970017607 FDA UDI
Primary DI / UDI-DI: 00733657202083 FDA UDI
FDA Product Code: CCX FDA UDI
GMDN Term: Limb/torso/head restraint, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.6820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Limb/torso/head restraint, reusable

Alistrap Maxx 10 In Wide X 30ft Long by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Limb/torso/head restraint, reusable.

E.M Adams co, inc. — E.M. Adams · Class I
E.M. Adams Co, Inc. — E.M. Adams · Class I
E.M. ADAMS CO, INC — E.M. Adams · Class I
POSEY — POSEY PRODUCTS, LLC · Class I
Morrison Medical — MORRISON MEDICAL, LTD · Class I
Restraint strap — Skytron, LLC · Class I
E.M Adams co, inc. — E.M. Adams · Class I
MORRISON MEDICAL — MORRISON MEDICAL, LTD · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: AliMed, LLC

Sources (1)

FDA UDI 3b10cd1b-c764-41d0-a905-6cda0401341a 34 fields · synced Jun 9, 2026