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30320 Reusable Body strap (2/pckg)

FDA UDI

Class I (US FDA UDI)

by Xodus Medical, Inc.

Identity

Trade Name
30320 Reusable Body strap (2/pckg) FDA UDI
Generic Name
Limb/torso/head restraint, single-use FDA UDI
Device Name
30320 Reusable Body strap (2/pckg) FDA UDI
Model / Reference
30320 FDA UDI
Description
30320 Reusable Body strap (2/pckg) FDA UDI

Identifiers

Catalog Number
30320 FDA UDI
Primary DI / UDI-DI
00787551011647 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Limb/torso/head restraint, single-use 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

30320 Reusable Body strap (2/pckg) by Xodus Medical, 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
Xodus Medical, Inc.

Sources (1)

  • FDA UDI aaff0fc2-6a47-4195-ad14-442aebd10d86 35 fields · synced Jun 1, 2026