Identity
- Trade Name
- Vive FDA UDI
- Generic Name
- Wrist binder, reusable FDA UDI
- Device Name
- Bamboo Wrist (Black) Large FDA UDI
- Model / Reference
- SUP1077L FDA UDI
- Description
- Bamboo Wrist (Black) Large FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00818323021943 FDA UDI
- FDA Product Code
- ILG FDA UDI
- GMDN Term
- Wrist binder, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3475 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Wrist binder, reusable
Vive by Vive Health Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wrist binder, reusable.
- Medline — MEDLINE INDUSTRIES, INC. · Class I
- Medline — MEDLINE INDUSTRIES, INC. · Class I
- Medline — MEDLINE INDUSTRIES, INC. · Class I
- Medline — MEDLINE INDUSTRIES, INC. · Class I
- Medline — MEDLINE INDUSTRIES, INC. · Class I
- M-Brace Air — INDACO SRL · Class I
- M-Brace Air — INDACO SRL · Class I
- Medline — MEDLINE INDUSTRIES, INC. · 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
- Vive Health Llc
Sources (1)
- FDA UDI 182aa8de-1151-473a-9741-5d6bd164c105 33 fields · synced Jun 8, 2026