Identity
- Trade Name
- Brasseler USA FDA UDI
- Generic Name
- Surgical binoculars, reusable FDA UDI
- Device Name
- VE TTL PRESCRIPTION RX ADD-ON FDA UDI
- Model / Reference
- 5029552U0 FDA UDI
- Description
- VE TTL PRESCRIPTION RX ADD-ON FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00887919933434 FDA UDI
- FDA Product Code
- FSP FDA UDI
- GMDN Term
- Surgical binoculars, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical binoculars, reusable
Brasseler USA by Peter Brasseler Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical binoculars, reusable.
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- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- SuperVu XL Advantage 3.5x, at 34cm working distanc — Rudolf Riester GmbH & Co. KG · Class I
- Surgical Telescope — Xenosys Co., Ltd. · Class I
- PENTAX PRISMVUE NF2 L25S(S) — HOYA Technosurgical Corporation · 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 |
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Manufacturer
- Manufacturer
- Peter Brasseler Holdings, LLC
Sources (1)
- FDA UDI e0188827-1db7-455a-b912-cfab5a55b1e5 33 fields · synced Jun 8, 2026